Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Clinical trials Research Evaluation). Showing records 1 – 30 of 87258 total matches.

[1] [2] [3] [4] [5] … [2909]

Search Limiters

Last 2 Years | English Only

Languages

Country

▼ Search Limiters


University of KwaZulu-Natal

1. [No author]. Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies.

Degree: 2012, University of KwaZulu-Natal

 Recent successes of antiretroviral pre-exposure prophylaxis (PrEP) in preventing HIV infection have raised questions whether further placebo controlled trials of new HIV-prevention technologies are ethically… (more)

Subjects/Keywords: Clinical trials.; Clinical trials – Ethics.; HIV infections – Research.; HIV infections – Prevention.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

author], [. (2012). Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies. (Thesis). University of KwaZulu-Natal. Retrieved from http://dx.doi.org/10.1097/QAD.0b013e3283509a29.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

author], [No. “Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies. ” 2012. Thesis, University of KwaZulu-Natal. Accessed November 22, 2019. http://dx.doi.org/10.1097/QAD.0b013e3283509a29..

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

author], [No. “Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies. ” 2012. Web. 22 Nov 2019.

Vancouver:

author] [. Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies. [Internet] [Thesis]. University of KwaZulu-Natal; 2012. [cited 2019 Nov 22]. Available from: http://dx.doi.org/10.1097/QAD.0b013e3283509a29..

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

author] [. Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies. [Thesis]. University of KwaZulu-Natal; 2012. Available from: http://dx.doi.org/10.1097/QAD.0b013e3283509a29.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hong Kong

2. Li, Hoi-kwong. Filing of complaints by the US Food and Drug Administration.

Degree: Master of Medical Sciences, 2005, University of Hong Kong

published_or_final_version

Medical Sciences

Master

Master of Medical Sciences

Subjects/Keywords: Clinical trials - Evaluation.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Li, H. (2005). Filing of complaints by the US Food and Drug Administration. (Masters Thesis). University of Hong Kong. Retrieved from Li, H. [李海光]. (2005). Filing of complaints by the US Food and Drug Administration. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4501076 ; http://dx.doi.org/10.5353/th_b4501076 ; http://hdl.handle.net/10722/131268

Chicago Manual of Style (16th Edition):

Li, Hoi-kwong. “Filing of complaints by the US Food and Drug Administration.” 2005. Masters Thesis, University of Hong Kong. Accessed November 22, 2019. Li, H. [李海光]. (2005). Filing of complaints by the US Food and Drug Administration. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4501076 ; http://dx.doi.org/10.5353/th_b4501076 ; http://hdl.handle.net/10722/131268.

MLA Handbook (7th Edition):

Li, Hoi-kwong. “Filing of complaints by the US Food and Drug Administration.” 2005. Web. 22 Nov 2019.

Vancouver:

Li H. Filing of complaints by the US Food and Drug Administration. [Internet] [Masters thesis]. University of Hong Kong; 2005. [cited 2019 Nov 22]. Available from: Li, H. [李海光]. (2005). Filing of complaints by the US Food and Drug Administration. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4501076 ; http://dx.doi.org/10.5353/th_b4501076 ; http://hdl.handle.net/10722/131268.

Council of Science Editors:

Li H. Filing of complaints by the US Food and Drug Administration. [Masters Thesis]. University of Hong Kong; 2005. Available from: Li, H. [李海光]. (2005). Filing of complaints by the US Food and Drug Administration. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4501076 ; http://dx.doi.org/10.5353/th_b4501076 ; http://hdl.handle.net/10722/131268


University of KwaZulu-Natal

3. [No author]. Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial.

Degree: 2011, University of KwaZulu-Natal

 Background—In settings where multiple HIV prevention trials are conducted in close proximity, trial participants may attempt to enroll in more than one trial simultaneously. Co-enrollment… (more)

Subjects/Keywords: Clinical trials – Social aspects.; AIDS (Disease) – Research.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

author], [. (2011). Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial. (Thesis). University of KwaZulu-Natal. Retrieved from http://dx.doi.org/10.1016/j.cct.2011.01.005.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

author], [No. “Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial. ” 2011. Thesis, University of KwaZulu-Natal. Accessed November 22, 2019. http://dx.doi.org/10.1016/j.cct.2011.01.005..

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

author], [No. “Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial. ” 2011. Web. 22 Nov 2019.

Vancouver:

author] [. Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial. [Internet] [Thesis]. University of KwaZulu-Natal; 2011. [cited 2019 Nov 22]. Available from: http://dx.doi.org/10.1016/j.cct.2011.01.005..

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

author] [. Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial. [Thesis]. University of KwaZulu-Natal; 2011. Available from: http://dx.doi.org/10.1016/j.cct.2011.01.005.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Vanderbilt University

4. Nagarsheth, Meera Bharat. A Critical Review of African Americanâs Recruitment in HIV/AIDS Clinical Trials: Why Sociostructural Context Matters.

Degree: MA, Medicine, Health, and Society, 2016, Vanderbilt University

 Despite being the racial/ethnic group that is disproportionately affected by HIV/AIDS, African Americans are underrepresented in HIV/AIDS clinical trials. The reasons for the inadequate participation… (more)

Subjects/Keywords: African Americans; HIV/AIDS; Clinical Trials Research

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Nagarsheth, M. B. (2016). A Critical Review of African Americanâs Recruitment in HIV/AIDS Clinical Trials: Why Sociostructural Context Matters. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-04182016-111137/ ;

Chicago Manual of Style (16th Edition):

Nagarsheth, Meera Bharat. “A Critical Review of African Americanâs Recruitment in HIV/AIDS Clinical Trials: Why Sociostructural Context Matters.” 2016. Masters Thesis, Vanderbilt University. Accessed November 22, 2019. http://etd.library.vanderbilt.edu/available/etd-04182016-111137/ ;.

MLA Handbook (7th Edition):

Nagarsheth, Meera Bharat. “A Critical Review of African Americanâs Recruitment in HIV/AIDS Clinical Trials: Why Sociostructural Context Matters.” 2016. Web. 22 Nov 2019.

Vancouver:

Nagarsheth MB. A Critical Review of African Americanâs Recruitment in HIV/AIDS Clinical Trials: Why Sociostructural Context Matters. [Internet] [Masters thesis]. Vanderbilt University; 2016. [cited 2019 Nov 22]. Available from: http://etd.library.vanderbilt.edu/available/etd-04182016-111137/ ;.

Council of Science Editors:

Nagarsheth MB. A Critical Review of African Americanâs Recruitment in HIV/AIDS Clinical Trials: Why Sociostructural Context Matters. [Masters Thesis]. Vanderbilt University; 2016. Available from: http://etd.library.vanderbilt.edu/available/etd-04182016-111137/ ;


University of Hong Kong

5. 馬詠恩.; Ma, Wing-yan. Contract research organizations: performance and evaluation of services.

Degree: MPH, 2006, University of Hong Kong

published_or_final_version

Community Medicine

Master

Master of Public Health

Subjects/Keywords: Pharmaceutical industry - Subcontracting.; Clinical trials - Subcontracting.; Drugs - Research - Evaluation.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

馬詠恩.; Ma, W. (2006). Contract research organizations: performance and evaluation of services. (Masters Thesis). University of Hong Kong. Retrieved from Ma, W. [馬詠恩]. (2006). Contract research organizations : performance and evaluation of services. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3972488 ; http://dx.doi.org/10.5353/th_b3972488 ; http://hdl.handle.net/10722/50765

Chicago Manual of Style (16th Edition):

馬詠恩.; Ma, Wing-yan. “Contract research organizations: performance and evaluation of services.” 2006. Masters Thesis, University of Hong Kong. Accessed November 22, 2019. Ma, W. [馬詠恩]. (2006). Contract research organizations : performance and evaluation of services. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3972488 ; http://dx.doi.org/10.5353/th_b3972488 ; http://hdl.handle.net/10722/50765.

MLA Handbook (7th Edition):

馬詠恩.; Ma, Wing-yan. “Contract research organizations: performance and evaluation of services.” 2006. Web. 22 Nov 2019.

Vancouver:

馬詠恩.; Ma W. Contract research organizations: performance and evaluation of services. [Internet] [Masters thesis]. University of Hong Kong; 2006. [cited 2019 Nov 22]. Available from: Ma, W. [馬詠恩]. (2006). Contract research organizations : performance and evaluation of services. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3972488 ; http://dx.doi.org/10.5353/th_b3972488 ; http://hdl.handle.net/10722/50765.

Council of Science Editors:

馬詠恩.; Ma W. Contract research organizations: performance and evaluation of services. [Masters Thesis]. University of Hong Kong; 2006. Available from: Ma, W. [馬詠恩]. (2006). Contract research organizations : performance and evaluation of services. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3972488 ; http://dx.doi.org/10.5353/th_b3972488 ; http://hdl.handle.net/10722/50765


University of Washington

6. Bennette, Caroline. Prioritizing research: the use of risk prediction, value of information analyses, and portfolio evaluation to improve public investments in cancer clinical trials.

Degree: PhD, 2015, University of Washington

 Background: Fewer than half of all medical interventions in use today are supported by clinical evidence. Despite allocating more than $11 billion each year to… (more)

Subjects/Keywords: cancer; clinical trials; portfolio evaluation; research prioritization; risk prediction; value of information; Public health; Economics; Health sciences; to be assigned

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bennette, C. (2015). Prioritizing research: the use of risk prediction, value of information analyses, and portfolio evaluation to improve public investments in cancer clinical trials. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/33083

Chicago Manual of Style (16th Edition):

Bennette, Caroline. “Prioritizing research: the use of risk prediction, value of information analyses, and portfolio evaluation to improve public investments in cancer clinical trials.” 2015. Doctoral Dissertation, University of Washington. Accessed November 22, 2019. http://hdl.handle.net/1773/33083.

MLA Handbook (7th Edition):

Bennette, Caroline. “Prioritizing research: the use of risk prediction, value of information analyses, and portfolio evaluation to improve public investments in cancer clinical trials.” 2015. Web. 22 Nov 2019.

Vancouver:

Bennette C. Prioritizing research: the use of risk prediction, value of information analyses, and portfolio evaluation to improve public investments in cancer clinical trials. [Internet] [Doctoral dissertation]. University of Washington; 2015. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1773/33083.

Council of Science Editors:

Bennette C. Prioritizing research: the use of risk prediction, value of information analyses, and portfolio evaluation to improve public investments in cancer clinical trials. [Doctoral Dissertation]. University of Washington; 2015. Available from: http://hdl.handle.net/1773/33083


Columbia University

7. Bothwell, Laura. The Emergence of the Randomized Controlled Trial: Origins to 1980.

Degree: 2014, Columbia University

 In received biomedical research wisdom, randomized controlled trials (RCTs) revolutionized post-World War II health research. By blending statistical analysis with the testing of new procedures… (more)

Subjects/Keywords: Medicine – Research; Clinical trials – Moral and ethical aspects; Clinical trials; Science; History; Ethics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bothwell, L. (2014). The Emergence of the Randomized Controlled Trial: Origins to 1980. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8K072V0

Chicago Manual of Style (16th Edition):

Bothwell, Laura. “The Emergence of the Randomized Controlled Trial: Origins to 1980.” 2014. Doctoral Dissertation, Columbia University. Accessed November 22, 2019. https://doi.org/10.7916/D8K072V0.

MLA Handbook (7th Edition):

Bothwell, Laura. “The Emergence of the Randomized Controlled Trial: Origins to 1980.” 2014. Web. 22 Nov 2019.

Vancouver:

Bothwell L. The Emergence of the Randomized Controlled Trial: Origins to 1980. [Internet] [Doctoral dissertation]. Columbia University; 2014. [cited 2019 Nov 22]. Available from: https://doi.org/10.7916/D8K072V0.

Council of Science Editors:

Bothwell L. The Emergence of the Randomized Controlled Trial: Origins to 1980. [Doctoral Dissertation]. Columbia University; 2014. Available from: https://doi.org/10.7916/D8K072V0


University of North Texas

8. Green, Asha M. Participant Perspectives: Investigating the Experience of Low-Income Schizophrenics in Clinical Research Trials.

Degree: 2015, University of North Texas

 The continued investigation into the experiences of individuals with schizophrenia who participate in biomedical research trials is necessary in order to understand participants’ perspectives, motivations,… (more)

Subjects/Keywords: clinical research trials; schizophrenia; participant feedback; Schizophrenics.; Clinical trials.; Poor.; Schizophrenia  – Treatment.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Green, A. M. (2015). Participant Perspectives: Investigating the Experience of Low-Income Schizophrenics in Clinical Research Trials. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc799519/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Green, Asha M. “Participant Perspectives: Investigating the Experience of Low-Income Schizophrenics in Clinical Research Trials.” 2015. Thesis, University of North Texas. Accessed November 22, 2019. https://digital.library.unt.edu/ark:/67531/metadc799519/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Green, Asha M. “Participant Perspectives: Investigating the Experience of Low-Income Schizophrenics in Clinical Research Trials.” 2015. Web. 22 Nov 2019.

Vancouver:

Green AM. Participant Perspectives: Investigating the Experience of Low-Income Schizophrenics in Clinical Research Trials. [Internet] [Thesis]. University of North Texas; 2015. [cited 2019 Nov 22]. Available from: https://digital.library.unt.edu/ark:/67531/metadc799519/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Green AM. Participant Perspectives: Investigating the Experience of Low-Income Schizophrenics in Clinical Research Trials. [Thesis]. University of North Texas; 2015. Available from: https://digital.library.unt.edu/ark:/67531/metadc799519/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of KwaZulu-Natal

9. Abdool Karim, Salim Safurdeen. Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies.

Degree: 2012, University of KwaZulu-Natal

 Recent successes of antiretroviral pre-exposure prophylaxis (PrEP) in preventing HIV infection have raised questions whether further placebo controlled trials of new HIV-prevention technologies are ethically… (more)

Subjects/Keywords: Clinical trials.; Clinical trials – Ethics.; HIV infections – Research.; HIV infections – Prevention.; Placebo controlled trials.; Antiretroviral pre-exposure prophylaxis (PrEP); Adherence.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Abdool Karim, S. S. (2012). Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/9184

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Abdool Karim, Salim Safurdeen. “Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies.” 2012. Thesis, University of KwaZulu-Natal. Accessed November 22, 2019. http://hdl.handle.net/10413/9184.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Abdool Karim, Salim Safurdeen. “Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies.” 2012. Web. 22 Nov 2019.

Vancouver:

Abdool Karim SS. Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies. [Internet] [Thesis]. University of KwaZulu-Natal; 2012. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10413/9184.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Abdool Karim SS. Design challenges facing clinical trials of the effectiveness of new HIV prevention technologies. [Thesis]. University of KwaZulu-Natal; 2012. Available from: http://hdl.handle.net/10413/9184

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of KwaZulu-Natal

10. McCormack, Sheena. Microbicide clinical trial adherence: insights for introduction.

Degree: 2013, University of KwaZulu-Natal

 After two decades of microbicide clinical trials it remains uncertain if vaginally- delivered products will be clearly shown to reduce the risk of HIV infection… (more)

Subjects/Keywords: Clinical trials – Research.; HIV infections – Prevention.; Vaginal microbicides.; Clinical trial adherence.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

McCormack, S. (2013). Microbicide clinical trial adherence: insights for introduction. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/9991

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

McCormack, Sheena. “Microbicide clinical trial adherence: insights for introduction.” 2013. Thesis, University of KwaZulu-Natal. Accessed November 22, 2019. http://hdl.handle.net/10413/9991.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

McCormack, Sheena. “Microbicide clinical trial adherence: insights for introduction.” 2013. Web. 22 Nov 2019.

Vancouver:

McCormack S. Microbicide clinical trial adherence: insights for introduction. [Internet] [Thesis]. University of KwaZulu-Natal; 2013. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10413/9991.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

McCormack S. Microbicide clinical trial adherence: insights for introduction. [Thesis]. University of KwaZulu-Natal; 2013. Available from: http://hdl.handle.net/10413/9991

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

11. Singh, Dominique. An expanded role for clinical coordinators in investigator initiated clinical trial research.

Degree: 2014, University of Saskatchewan

Clinical research is conducted to advance human medicine by developing efficacious treatments and improving patient outcomes when new therapies are developed and implemented. Clinical trials(more)

Subjects/Keywords: Clinical research; Registered Nurse; Clinical Coordinator; investigator-initiated clinical trials; good clinical practice; adhesions

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Singh, D. (2014). An expanded role for clinical coordinators in investigator initiated clinical trial research. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2014-11-1850

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Singh, Dominique. “An expanded role for clinical coordinators in investigator initiated clinical trial research.” 2014. Thesis, University of Saskatchewan. Accessed November 22, 2019. http://hdl.handle.net/10388/ETD-2014-11-1850.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Singh, Dominique. “An expanded role for clinical coordinators in investigator initiated clinical trial research.” 2014. Web. 22 Nov 2019.

Vancouver:

Singh D. An expanded role for clinical coordinators in investigator initiated clinical trial research. [Internet] [Thesis]. University of Saskatchewan; 2014. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10388/ETD-2014-11-1850.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Singh D. An expanded role for clinical coordinators in investigator initiated clinical trial research. [Thesis]. University of Saskatchewan; 2014. Available from: http://hdl.handle.net/10388/ETD-2014-11-1850

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Oxford

12. Chan, An-Wen. Outcome reporting bias in randomised trials : implications for systematic reviews.

Degree: PhD, 2003, University of Oxford

 Background Selective reporting of outcomes within a published study based on their nature or direction can result in systematic differences between reported and unreported data.… (more)

Subjects/Keywords: 610.72; Clinical trials; Evaluation; Medicine; Research; Systematic reviews (Medical research); Evidence-based medicine

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Chan, A. (2003). Outcome reporting bias in randomised trials : implications for systematic reviews. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:8149b902-cb7f-487b-b187-67604eb87463 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618374

Chicago Manual of Style (16th Edition):

Chan, An-Wen. “Outcome reporting bias in randomised trials : implications for systematic reviews.” 2003. Doctoral Dissertation, University of Oxford. Accessed November 22, 2019. http://ora.ox.ac.uk/objects/uuid:8149b902-cb7f-487b-b187-67604eb87463 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618374.

MLA Handbook (7th Edition):

Chan, An-Wen. “Outcome reporting bias in randomised trials : implications for systematic reviews.” 2003. Web. 22 Nov 2019.

Vancouver:

Chan A. Outcome reporting bias in randomised trials : implications for systematic reviews. [Internet] [Doctoral dissertation]. University of Oxford; 2003. [cited 2019 Nov 22]. Available from: http://ora.ox.ac.uk/objects/uuid:8149b902-cb7f-487b-b187-67604eb87463 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618374.

Council of Science Editors:

Chan A. Outcome reporting bias in randomised trials : implications for systematic reviews. [Doctoral Dissertation]. University of Oxford; 2003. Available from: http://ora.ox.ac.uk/objects/uuid:8149b902-cb7f-487b-b187-67604eb87463 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618374

13. Saeed, Iman. Comparison of Methods for Handling Missing Outcome Data in Randomized Controlled Trials.

Degree: Department of Biostatistics, 2017, Brown University

 Background: Randomized clinical trials (RCTs) are considered the gold standard approach for assessing the comparative effectiveness of medical interventions. Given the importance of RCTs for… (more)

Subjects/Keywords: Clinical trials

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Saeed, I. (2017). Comparison of Methods for Handling Missing Outcome Data in Randomized Controlled Trials. (Thesis). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:733496/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Saeed, Iman. “Comparison of Methods for Handling Missing Outcome Data in Randomized Controlled Trials.” 2017. Thesis, Brown University. Accessed November 22, 2019. https://repository.library.brown.edu/studio/item/bdr:733496/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Saeed, Iman. “Comparison of Methods for Handling Missing Outcome Data in Randomized Controlled Trials.” 2017. Web. 22 Nov 2019.

Vancouver:

Saeed I. Comparison of Methods for Handling Missing Outcome Data in Randomized Controlled Trials. [Internet] [Thesis]. Brown University; 2017. [cited 2019 Nov 22]. Available from: https://repository.library.brown.edu/studio/item/bdr:733496/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Saeed I. Comparison of Methods for Handling Missing Outcome Data in Randomized Controlled Trials. [Thesis]. Brown University; 2017. Available from: https://repository.library.brown.edu/studio/item/bdr:733496/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Rutgers University

14. Gu, Hui, 1984-. Two-stage design for phase II cancer clinical trials with multiple endpoints.

Degree: PhD, Public Health, 2017, Rutgers University

The main purpose of a single-arm phase II cancer trial of a new regimen is to determine whether it has sufficient anti-tumor activity against a… (more)

Subjects/Keywords: Clinical trials

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Gu, Hui, 1. (2017). Two-stage design for phase II cancer clinical trials with multiple endpoints. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/55504/

Chicago Manual of Style (16th Edition):

Gu, Hui, 1984-. “Two-stage design for phase II cancer clinical trials with multiple endpoints.” 2017. Doctoral Dissertation, Rutgers University. Accessed November 22, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/55504/.

MLA Handbook (7th Edition):

Gu, Hui, 1984-. “Two-stage design for phase II cancer clinical trials with multiple endpoints.” 2017. Web. 22 Nov 2019.

Vancouver:

Gu, Hui 1. Two-stage design for phase II cancer clinical trials with multiple endpoints. [Internet] [Doctoral dissertation]. Rutgers University; 2017. [cited 2019 Nov 22]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55504/.

Council of Science Editors:

Gu, Hui 1. Two-stage design for phase II cancer clinical trials with multiple endpoints. [Doctoral Dissertation]. Rutgers University; 2017. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55504/


University of Oxford

15. Brice, Anne. Mapping the uncertainties in internet-based clinical trials : a systematic review and qualitative study.

Degree: PhD, 2017, University of Oxford

 This thesis maps the growth of the use of internet technologies in randomised controlled trials in health care and public health, and explores the methodological… (more)

Subjects/Keywords: Internet-based clinical trials; Qualitative research; Participant experience; Researcher experience; Randomised controlled trials; Internet

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Brice, A. (2017). Mapping the uncertainties in internet-based clinical trials : a systematic review and qualitative study. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:8a24b79f-6629-482d-b5a4-543f8ce7b07f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736068

Chicago Manual of Style (16th Edition):

Brice, Anne. “Mapping the uncertainties in internet-based clinical trials : a systematic review and qualitative study.” 2017. Doctoral Dissertation, University of Oxford. Accessed November 22, 2019. http://ora.ox.ac.uk/objects/uuid:8a24b79f-6629-482d-b5a4-543f8ce7b07f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736068.

MLA Handbook (7th Edition):

Brice, Anne. “Mapping the uncertainties in internet-based clinical trials : a systematic review and qualitative study.” 2017. Web. 22 Nov 2019.

Vancouver:

Brice A. Mapping the uncertainties in internet-based clinical trials : a systematic review and qualitative study. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2019 Nov 22]. Available from: http://ora.ox.ac.uk/objects/uuid:8a24b79f-6629-482d-b5a4-543f8ce7b07f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736068.

Council of Science Editors:

Brice A. Mapping the uncertainties in internet-based clinical trials : a systematic review and qualitative study. [Doctoral Dissertation]. University of Oxford; 2017. Available from: http://ora.ox.ac.uk/objects/uuid:8a24b79f-6629-482d-b5a4-543f8ce7b07f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736068


University of Southern California

16. Whalen, Ellen R. Clinical trials driven by investigator-sponsors: GCP compliance with or without previous industry sponsorship.

Degree: Doctor of Regulatory Science, Regulatory Science, 2013, University of Southern California

 The present study was conducted to evaluate using the Plan-Do-Check-Act cycle (PDCA) typical of quality control systems to evaluate the state of compliance with Good… (more)

Subjects/Keywords: clinical research quality control; clinical trials; GCP compliance; good clinical practices; PDCA cycle; sponsor-investigators

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Whalen, E. R. (2013). Clinical trials driven by investigator-sponsors: GCP compliance with or without previous industry sponsorship. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/218930/rec/1386

Chicago Manual of Style (16th Edition):

Whalen, Ellen R. “Clinical trials driven by investigator-sponsors: GCP compliance with or without previous industry sponsorship.” 2013. Doctoral Dissertation, University of Southern California. Accessed November 22, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/218930/rec/1386.

MLA Handbook (7th Edition):

Whalen, Ellen R. “Clinical trials driven by investigator-sponsors: GCP compliance with or without previous industry sponsorship.” 2013. Web. 22 Nov 2019.

Vancouver:

Whalen ER. Clinical trials driven by investigator-sponsors: GCP compliance with or without previous industry sponsorship. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Nov 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/218930/rec/1386.

Council of Science Editors:

Whalen ER. Clinical trials driven by investigator-sponsors: GCP compliance with or without previous industry sponsorship. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/218930/rec/1386


IUPUI

17. Li, Claire. Modeling and simulation applications with potential impact in drug development and patient care.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Model-based drug development has become an essential element to potentially make drug development more productive by assessing the data using… (more)

Subjects/Keywords: modeling and simulation; pharmacokinetics; pharmacodynamics; genetics; Molecular pharmacology  – Research  – Evaluation  – Methodology; Drug development  – Pharmacokinetics; Drug development  – Molecular genetics; Drugs  – Physiological effect  – Mathematical models; Simulation methods  – Research  – Evaluation  – Methodology; Mathematical models  – Research  – Evaluation  – Methodology; Drugs  – Metabolism; Drugs  – Design; Clinical trials  – Research  – Evaluation; Drugs  – Testing; Drugs  – Toxicology; Patient-centered health care; Pharmacokinetics  – Research

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Li, C. (2014). Modeling and simulation applications with potential impact in drug development and patient care. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/5969

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Li, Claire. “Modeling and simulation applications with potential impact in drug development and patient care.” 2014. Thesis, IUPUI. Accessed November 22, 2019. http://hdl.handle.net/1805/5969.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Li, Claire. “Modeling and simulation applications with potential impact in drug development and patient care.” 2014. Web. 22 Nov 2019.

Vancouver:

Li C. Modeling and simulation applications with potential impact in drug development and patient care. [Internet] [Thesis]. IUPUI; 2014. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1805/5969.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Li C. Modeling and simulation applications with potential impact in drug development and patient care. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/5969

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Sydney

18. Ghersi, Davina. Issues in the design, conduct and reporting of clinical trials that impact on the quality of decision making .

Degree: 2006, University of Sydney

Subjects/Keywords: Clinical trials; Clinical trials  – Design; Clinical trials  – Decision making; Clinical trials  – Methodology; Clinical trials  – Technique; Decision making; Research  – Decision making

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ghersi, D. (2006). Issues in the design, conduct and reporting of clinical trials that impact on the quality of decision making . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/6653

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ghersi, Davina. “Issues in the design, conduct and reporting of clinical trials that impact on the quality of decision making .” 2006. Thesis, University of Sydney. Accessed November 22, 2019. http://hdl.handle.net/2123/6653.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ghersi, Davina. “Issues in the design, conduct and reporting of clinical trials that impact on the quality of decision making .” 2006. Web. 22 Nov 2019.

Vancouver:

Ghersi D. Issues in the design, conduct and reporting of clinical trials that impact on the quality of decision making . [Internet] [Thesis]. University of Sydney; 2006. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/2123/6653.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ghersi D. Issues in the design, conduct and reporting of clinical trials that impact on the quality of decision making . [Thesis]. University of Sydney; 2006. Available from: http://hdl.handle.net/2123/6653

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of KwaZulu-Natal

19. Abdool Karim, Salim Safurdeen. Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial.

Degree: 2011, University of KwaZulu-Natal

 Background: Young women in sub-Saharan Africa bear a disproportionate burden of HIV infection compared to men but have limited options to reduce their HIV risk.… (more)

Subjects/Keywords: Biomedical research.; Clinical trials.; HIV infections – Prevention – South Africa.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Abdool Karim, S. S. (2011). Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/7852

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Abdool Karim, Salim Safurdeen. “Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial.” 2011. Thesis, University of KwaZulu-Natal. Accessed November 22, 2019. http://hdl.handle.net/10413/7852.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Abdool Karim, Salim Safurdeen. “Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial.” 2011. Web. 22 Nov 2019.

Vancouver:

Abdool Karim SS. Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial. [Internet] [Thesis]. University of KwaZulu-Natal; 2011. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10413/7852.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Abdool Karim SS. Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial. [Thesis]. University of KwaZulu-Natal; 2011. Available from: http://hdl.handle.net/10413/7852

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of KwaZulu-Natal

20. [No author]. Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial.

Degree: 2011, University of KwaZulu-Natal

 Background: Young women in sub-Saharan Africa bear a disproportionate burden of HIV infection compared to men but have limited options to reduce their HIV risk.… (more)

Subjects/Keywords: Biomedical research.; Clinical trials.; HIV infections – Prevention – South Africa.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

author], [. (2011). Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial. (Thesis). University of KwaZulu-Natal. Retrieved from http://dx.doi.org/10.1186/1745-6215-12-67

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

author], [No. “Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial. ” 2011. Thesis, University of KwaZulu-Natal. Accessed November 22, 2019. http://dx.doi.org/10.1186/1745-6215-12-67.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

author], [No. “Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial. ” 2011. Web. 22 Nov 2019.

Vancouver:

author] [. Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial. [Internet] [Thesis]. University of KwaZulu-Natal; 2011. [cited 2019 Nov 22]. Available from: http://dx.doi.org/10.1186/1745-6215-12-67.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

author] [. Recruitment of high risk women for HIV prevention trials: baseline HIV prevalence and sexual behavior in the CAPRISA 004 tenofovir gel trial. [Thesis]. University of KwaZulu-Natal; 2011. Available from: http://dx.doi.org/10.1186/1745-6215-12-67

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hong Kong

21. 葉克剛; Yip, Hak-kong. A critical review of clinical trials in dental research.

Degree: Master of Medical Sciences, 1999, University of Hong Kong

published_or_final_version

Medical Sciences

Master

Master of Medical Sciences

Subjects/Keywords: Dentistry - Research.; Clinical trials

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

葉克剛; Yip, H. (1999). A critical review of clinical trials in dental research. (Masters Thesis). University of Hong Kong. Retrieved from Yip, H. [葉克剛]. (1999). A critical review of clinical trials in dental research. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3196989 ; http://dx.doi.org/10.5353/th_b3196989 ; http://hdl.handle.net/10722/25848

Chicago Manual of Style (16th Edition):

葉克剛; Yip, Hak-kong. “A critical review of clinical trials in dental research.” 1999. Masters Thesis, University of Hong Kong. Accessed November 22, 2019. Yip, H. [葉克剛]. (1999). A critical review of clinical trials in dental research. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3196989 ; http://dx.doi.org/10.5353/th_b3196989 ; http://hdl.handle.net/10722/25848.

MLA Handbook (7th Edition):

葉克剛; Yip, Hak-kong. “A critical review of clinical trials in dental research.” 1999. Web. 22 Nov 2019.

Vancouver:

葉克剛; Yip H. A critical review of clinical trials in dental research. [Internet] [Masters thesis]. University of Hong Kong; 1999. [cited 2019 Nov 22]. Available from: Yip, H. [葉克剛]. (1999). A critical review of clinical trials in dental research. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3196989 ; http://dx.doi.org/10.5353/th_b3196989 ; http://hdl.handle.net/10722/25848.

Council of Science Editors:

葉克剛; Yip H. A critical review of clinical trials in dental research. [Masters Thesis]. University of Hong Kong; 1999. Available from: Yip, H. [葉克剛]. (1999). A critical review of clinical trials in dental research. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3196989 ; http://dx.doi.org/10.5353/th_b3196989 ; http://hdl.handle.net/10722/25848


Baylor University

22. Hetzer, Joel D. Statistical considerations in the analysis of multivariate Phase II testing.

Degree: Statistical Sciences., 2009, Baylor University

 In medical diagnosis and treatment, many diseases are characterized by multiple measurable differences in clinical (e.g., physical or radiological differences) and laboratory parameters (biomarkers from… (more)

Subjects/Keywords: Clinical trials  – Statistical methods.; Multivariate analysis.; Metabolic syndrome  – Research  – Statistical methods.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Hetzer, J. D. (2009). Statistical considerations in the analysis of multivariate Phase II testing. (Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/5277

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hetzer, Joel D. “Statistical considerations in the analysis of multivariate Phase II testing. ” 2009. Thesis, Baylor University. Accessed November 22, 2019. http://hdl.handle.net/2104/5277.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hetzer, Joel D. “Statistical considerations in the analysis of multivariate Phase II testing. ” 2009. Web. 22 Nov 2019.

Vancouver:

Hetzer JD. Statistical considerations in the analysis of multivariate Phase II testing. [Internet] [Thesis]. Baylor University; 2009. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/2104/5277.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hetzer JD. Statistical considerations in the analysis of multivariate Phase II testing. [Thesis]. Baylor University; 2009. Available from: http://hdl.handle.net/2104/5277

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Rutgers University

23. Chen, Menghui. Dose finding methods based on cure rate model in phase I cancer clinical trials.

Degree: PhD, Statistics and Biostatistics, 2015, Rutgers University

The main goal of a Phase I cancer clinical trial is to identify the maximum tolerated dose (MTD) of a new drug having acceptable dose-limiting… (more)

Subjects/Keywords: Clinical trials; Cancer – Research; Cancer – Treatment; Drugs – Dose-response relationship

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Chen, M. (2015). Dose finding methods based on cure rate model in phase I cancer clinical trials. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/47337/

Chicago Manual of Style (16th Edition):

Chen, Menghui. “Dose finding methods based on cure rate model in phase I cancer clinical trials.” 2015. Doctoral Dissertation, Rutgers University. Accessed November 22, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/47337/.

MLA Handbook (7th Edition):

Chen, Menghui. “Dose finding methods based on cure rate model in phase I cancer clinical trials.” 2015. Web. 22 Nov 2019.

Vancouver:

Chen M. Dose finding methods based on cure rate model in phase I cancer clinical trials. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2019 Nov 22]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/47337/.

Council of Science Editors:

Chen M. Dose finding methods based on cure rate model in phase I cancer clinical trials. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/47337/


McMaster University

24. Ye, Chenglin. STATISTICAL AND METHODOLOGICAL ISSUES IN EVALUATION OF INTEGRATED CARE PROGRAMS.

Degree: PhD, 2014, McMaster University

Background Integrated care programs are collaborations to improve health services delivery for patients with multiple conditions. Objectives This thesis investigated three issues in evaluation(more)

Subjects/Keywords: Biostatistics; Clinical Epidemiology; Clinical Trials; Integrated care; Statistical Methodology; Health Research Methodology; Applied Statistics; Biostatistics; Clinical Epidemiology; Clinical Trials; Health Services Research; Statistical Methodology; Statistical Models; Applied Statistics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ye, C. (2014). STATISTICAL AND METHODOLOGICAL ISSUES IN EVALUATION OF INTEGRATED CARE PROGRAMS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/14124

Chicago Manual of Style (16th Edition):

Ye, Chenglin. “STATISTICAL AND METHODOLOGICAL ISSUES IN EVALUATION OF INTEGRATED CARE PROGRAMS.” 2014. Doctoral Dissertation, McMaster University. Accessed November 22, 2019. http://hdl.handle.net/11375/14124.

MLA Handbook (7th Edition):

Ye, Chenglin. “STATISTICAL AND METHODOLOGICAL ISSUES IN EVALUATION OF INTEGRATED CARE PROGRAMS.” 2014. Web. 22 Nov 2019.

Vancouver:

Ye C. STATISTICAL AND METHODOLOGICAL ISSUES IN EVALUATION OF INTEGRATED CARE PROGRAMS. [Internet] [Doctoral dissertation]. McMaster University; 2014. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/11375/14124.

Council of Science Editors:

Ye C. STATISTICAL AND METHODOLOGICAL ISSUES IN EVALUATION OF INTEGRATED CARE PROGRAMS. [Doctoral Dissertation]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/14124


Eastern Michigan University

25. Felemban, Rania Mohammad. Are clinical research professionals more inclined to participate in clinical trials?.

Degree: MS, Health Sciences, 2017, Eastern Michigan University

  The objective of this study was to identify the impact of professional knowledge and education on a willingness to participate in clinical trials. It… (more)

Subjects/Keywords: Clinical Research Professionals; Clinical Trials; Participate; Post-graduate; Professional background; Pharmacy and Pharmaceutical Sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Felemban, R. M. (2017). Are clinical research professionals more inclined to participate in clinical trials?. (Masters Thesis). Eastern Michigan University. Retrieved from http://commons.emich.edu/theses/727

Chicago Manual of Style (16th Edition):

Felemban, Rania Mohammad. “Are clinical research professionals more inclined to participate in clinical trials?.” 2017. Masters Thesis, Eastern Michigan University. Accessed November 22, 2019. http://commons.emich.edu/theses/727.

MLA Handbook (7th Edition):

Felemban, Rania Mohammad. “Are clinical research professionals more inclined to participate in clinical trials?.” 2017. Web. 22 Nov 2019.

Vancouver:

Felemban RM. Are clinical research professionals more inclined to participate in clinical trials?. [Internet] [Masters thesis]. Eastern Michigan University; 2017. [cited 2019 Nov 22]. Available from: http://commons.emich.edu/theses/727.

Council of Science Editors:

Felemban RM. Are clinical research professionals more inclined to participate in clinical trials?. [Masters Thesis]. Eastern Michigan University; 2017. Available from: http://commons.emich.edu/theses/727


University of KwaZulu-Natal

26. El-Sadr, Wafaa. Lessons from a randomised clinical trial for multidrug-resistant tuberculosis.

Degree: 2012, University of KwaZulu-Natal

 BACKGROUND: The treatment of multidrug-resistant tuberculosis (MDR-TB) is currently based upon expert opinion and findings from case series, rather than upon randomised clinical trials (RCTs).… (more)

Subjects/Keywords: Multidrug-resistant tuberculosis – Treatment.; Clinical trials – Evaluation.; HIV infections – Complications.; MDR-TB.; Tuberculosis Trials Consortium (TBTC) Study 30.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

El-Sadr, W. (2012). Lessons from a randomised clinical trial for multidrug-resistant tuberculosis. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/9245

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

El-Sadr, Wafaa. “Lessons from a randomised clinical trial for multidrug-resistant tuberculosis.” 2012. Thesis, University of KwaZulu-Natal. Accessed November 22, 2019. http://hdl.handle.net/10413/9245.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

El-Sadr, Wafaa. “Lessons from a randomised clinical trial for multidrug-resistant tuberculosis.” 2012. Web. 22 Nov 2019.

Vancouver:

El-Sadr W. Lessons from a randomised clinical trial for multidrug-resistant tuberculosis. [Internet] [Thesis]. University of KwaZulu-Natal; 2012. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10413/9245.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

El-Sadr W. Lessons from a randomised clinical trial for multidrug-resistant tuberculosis. [Thesis]. University of KwaZulu-Natal; 2012. Available from: http://hdl.handle.net/10413/9245

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Aberdeen

27. McPherson, Gladys. The role of minimisation in treatment allocation for clinical trials.

Degree: 2011, University of Aberdeen

 Simple randomisation is the easiest method for allocating participants to treatment groups in clinical trials. In the long run it balances all features of participants… (more)

Subjects/Keywords: 610.21; Clinical trials

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

McPherson, G. (2011). The role of minimisation in treatment allocation for clinical trials. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=167718 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542643

Chicago Manual of Style (16th Edition):

McPherson, Gladys. “The role of minimisation in treatment allocation for clinical trials.” 2011. Doctoral Dissertation, University of Aberdeen. Accessed November 22, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=167718 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542643.

MLA Handbook (7th Edition):

McPherson, Gladys. “The role of minimisation in treatment allocation for clinical trials.” 2011. Web. 22 Nov 2019.

Vancouver:

McPherson G. The role of minimisation in treatment allocation for clinical trials. [Internet] [Doctoral dissertation]. University of Aberdeen; 2011. [cited 2019 Nov 22]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=167718 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542643.

Council of Science Editors:

McPherson G. The role of minimisation in treatment allocation for clinical trials. [Doctoral Dissertation]. University of Aberdeen; 2011. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=167718 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542643


University of Toronto

28. Pham, Quynh. Innovative Research Methods to Evaluate Effective Engagement with Consumer Mobile Health Applications for Chronic Conditions.

Degree: PhD, 2019, University of Toronto

 Consumer mobile health applications (mHealth apps) hold enormous potential to provide effective, efficient, economical, and scalable chronic health care. The opportunities afforded by these interventions… (more)

Subjects/Keywords: digital health; health services research; innovative clinical trials; mobile health; research analytics; 0566

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Pham, Q. (2019). Innovative Research Methods to Evaluate Effective Engagement with Consumer Mobile Health Applications for Chronic Conditions. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/97584

Chicago Manual of Style (16th Edition):

Pham, Quynh. “Innovative Research Methods to Evaluate Effective Engagement with Consumer Mobile Health Applications for Chronic Conditions.” 2019. Doctoral Dissertation, University of Toronto. Accessed November 22, 2019. http://hdl.handle.net/1807/97584.

MLA Handbook (7th Edition):

Pham, Quynh. “Innovative Research Methods to Evaluate Effective Engagement with Consumer Mobile Health Applications for Chronic Conditions.” 2019. Web. 22 Nov 2019.

Vancouver:

Pham Q. Innovative Research Methods to Evaluate Effective Engagement with Consumer Mobile Health Applications for Chronic Conditions. [Internet] [Doctoral dissertation]. University of Toronto; 2019. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1807/97584.

Council of Science Editors:

Pham Q. Innovative Research Methods to Evaluate Effective Engagement with Consumer Mobile Health Applications for Chronic Conditions. [Doctoral Dissertation]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/97584


University of KwaZulu-Natal

29. Abdool Karim, Salim Safurdeen. Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial.

Degree: 2011, University of KwaZulu-Natal

 Background—In settings where multiple HIV prevention trials are conducted in close proximity, trial participants may attempt to enroll in more than one trial simultaneously. Co-enrollment… (more)

Subjects/Keywords: Clinical trials – Social aspects.; AIDS (Disease) – Research.; CAPRISA 004 Tenofovir gel trial.; HIV prevention trials.; Co-enrollment.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Abdool Karim, S. S. (2011). Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/9260

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Abdool Karim, Salim Safurdeen. “Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial.” 2011. Thesis, University of KwaZulu-Natal. Accessed November 22, 2019. http://hdl.handle.net/10413/9260.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Abdool Karim, Salim Safurdeen. “Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial.” 2011. Web. 22 Nov 2019.

Vancouver:

Abdool Karim SS. Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial. [Internet] [Thesis]. University of KwaZulu-Natal; 2011. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10413/9260.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Abdool Karim SS. Co-enrollment in multiple HIV prevention trials - experiences from the CAPRISA 004 Tenofovir gel trial. [Thesis]. University of KwaZulu-Natal; 2011. Available from: http://hdl.handle.net/10413/9260

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

30. Paschoale, Helena Scavone. Perfil da pesquisa clínica: identificação de oportunidades e desafios para o futuro.

Degree: Mestrado, Gastroenterologia Clínica, 2009, University of São Paulo

 A pesquisa clínica é considerada um método inovador em medicina clínica e essencial para o desenvolvimento de novas drogas. No Brasil, a pesquisa clínica teve… (more)

Subjects/Keywords: Clinical protocols; Clinical research/trends; Clinical trials; Ensaio clínico; Estudos transversais; Pesquisa biomédica/tendências; Protocolos clínicos; Questionários; Questionnaires; Transversal studies

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Paschoale, H. S. (2009). Perfil da pesquisa clínica: identificação de oportunidades e desafios para o futuro. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5147/tde-07122009-182348/ ;

Chicago Manual of Style (16th Edition):

Paschoale, Helena Scavone. “Perfil da pesquisa clínica: identificação de oportunidades e desafios para o futuro.” 2009. Masters Thesis, University of São Paulo. Accessed November 22, 2019. http://www.teses.usp.br/teses/disponiveis/5/5147/tde-07122009-182348/ ;.

MLA Handbook (7th Edition):

Paschoale, Helena Scavone. “Perfil da pesquisa clínica: identificação de oportunidades e desafios para o futuro.” 2009. Web. 22 Nov 2019.

Vancouver:

Paschoale HS. Perfil da pesquisa clínica: identificação de oportunidades e desafios para o futuro. [Internet] [Masters thesis]. University of São Paulo; 2009. [cited 2019 Nov 22]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5147/tde-07122009-182348/ ;.

Council of Science Editors:

Paschoale HS. Perfil da pesquisa clínica: identificação de oportunidades e desafios para o futuro. [Masters Thesis]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/5/5147/tde-07122009-182348/ ;

[1] [2] [3] [4] [5] … [2909]

.