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You searched for subject:(Clinical trials). Showing records 1 – 30 of 574 total matches.

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1. 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

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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 October 26, 2020. 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. 26 Oct 2020.

Vancouver:

Saeed I. Comparison of Methods for Handling Missing Outcome Data in Randomized Controlled Trials. [Internet] [Thesis]. Brown University; 2017. [cited 2020 Oct 26]. 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

2. 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

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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 October 26, 2020. 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. 26 Oct 2020.

Vancouver:

Gu, Hui 1. Two-stage design for phase II cancer clinical trials with multiple endpoints. [Internet] [Doctoral dissertation]. Rutgers University; 2017. [cited 2020 Oct 26]. 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 Aberdeen

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

Degree: PhD, 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

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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 October 26, 2020. 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. 26 Oct 2020.

Vancouver:

McPherson G. The role of minimisation in treatment allocation for clinical trials. [Internet] [Doctoral dissertation]. University of Aberdeen; 2011. [cited 2020 Oct 26]. 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 Aberdeen

4. Gardner, Heidi. Making clinical trials more efficient : consolidating, communicating and improving knowledge of participant recruitment interventions.

Degree: PhD, 2018, University of Aberdeen

 Why was the research in this thesis done? Recruitment of participants is an important part of trials, but the evidence that is available to help… (more)

Subjects/Keywords: Clinical trials; Medicine

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APA (6th Edition):

Gardner, H. (2018). Making clinical trials more efficient : consolidating, communicating and improving knowledge of participant recruitment interventions. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=239193 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801250

Chicago Manual of Style (16th Edition):

Gardner, Heidi. “Making clinical trials more efficient : consolidating, communicating and improving knowledge of participant recruitment interventions.” 2018. Doctoral Dissertation, University of Aberdeen. Accessed October 26, 2020. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=239193 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801250.

MLA Handbook (7th Edition):

Gardner, Heidi. “Making clinical trials more efficient : consolidating, communicating and improving knowledge of participant recruitment interventions.” 2018. Web. 26 Oct 2020.

Vancouver:

Gardner H. Making clinical trials more efficient : consolidating, communicating and improving knowledge of participant recruitment interventions. [Internet] [Doctoral dissertation]. University of Aberdeen; 2018. [cited 2020 Oct 26]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=239193 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801250.

Council of Science Editors:

Gardner H. Making clinical trials more efficient : consolidating, communicating and improving knowledge of participant recruitment interventions. [Doctoral Dissertation]. University of Aberdeen; 2018. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=239193 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801250


University of Hong Kong

5. Teh, Jun-chuan. Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP.

Degree: 2007, University of Hong Kong

Subjects/Keywords: Clinical trials.

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

APA (6th Edition):

Teh, J. (2007). Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/50768

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):

Teh, Jun-chuan. “Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP.” 2007. Thesis, University of Hong Kong. Accessed October 26, 2020. http://hdl.handle.net/10722/50768.

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

MLA Handbook (7th Edition):

Teh, Jun-chuan. “Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP.” 2007. Web. 26 Oct 2020.

Vancouver:

Teh J. Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP. [Internet] [Thesis]. University of Hong Kong; 2007. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/10722/50768.

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

Council of Science Editors:

Teh J. Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP. [Thesis]. University of Hong Kong; 2007. Available from: http://hdl.handle.net/10722/50768

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


University of Wollongong

6. Jameson, Michael Geoffrey. Hitting the target: analysis of delineation and dosimetric uncertainty in radiotherapy.

Degree: PhD, 2015, University of Wollongong

  Through advances in radiation delivery systems and image guidance, the accuracy and precision of radiation therapy has improved in recent times. Some aspects with… (more)

Subjects/Keywords: radiotherapy; uncertainty; contouring; clinical trials

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APA (6th Edition):

Jameson, M. G. (2015). Hitting the target: analysis of delineation and dosimetric uncertainty in radiotherapy. (Doctoral Dissertation). University of Wollongong. Retrieved from 0299 OTHER PHYSICAL SCIENCES, 1103 CLINICAL SCIENCES, 1112 ONCOLOGY AND CARCINOGENESIS ; https://ro.uow.edu.au/theses/4607

Chicago Manual of Style (16th Edition):

Jameson, Michael Geoffrey. “Hitting the target: analysis of delineation and dosimetric uncertainty in radiotherapy.” 2015. Doctoral Dissertation, University of Wollongong. Accessed October 26, 2020. 0299 OTHER PHYSICAL SCIENCES, 1103 CLINICAL SCIENCES, 1112 ONCOLOGY AND CARCINOGENESIS ; https://ro.uow.edu.au/theses/4607.

MLA Handbook (7th Edition):

Jameson, Michael Geoffrey. “Hitting the target: analysis of delineation and dosimetric uncertainty in radiotherapy.” 2015. Web. 26 Oct 2020.

Vancouver:

Jameson MG. Hitting the target: analysis of delineation and dosimetric uncertainty in radiotherapy. [Internet] [Doctoral dissertation]. University of Wollongong; 2015. [cited 2020 Oct 26]. Available from: 0299 OTHER PHYSICAL SCIENCES, 1103 CLINICAL SCIENCES, 1112 ONCOLOGY AND CARCINOGENESIS ; https://ro.uow.edu.au/theses/4607.

Council of Science Editors:

Jameson MG. Hitting the target: analysis of delineation and dosimetric uncertainty in radiotherapy. [Doctoral Dissertation]. University of Wollongong; 2015. Available from: 0299 OTHER PHYSICAL SCIENCES, 1103 CLINICAL SCIENCES, 1112 ONCOLOGY AND CARCINOGENESIS ; https://ro.uow.edu.au/theses/4607


University of Aberdeen

7. McGhee, David J. M. Improving clinical trial design in neurodegenerative disorders.

Degree: PhD, 2014, University of Aberdeen

 This thesis aimed to improve the methodology of disease-modification clinical trials in neurodegenerative disorders, with particular reference to Parkinson's disease (PD) and Alzheimer's disease. A… (more)

Subjects/Keywords: 616.8; Nervous system; Clinical trials

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APA (6th Edition):

McGhee, D. J. M. (2014). Improving clinical trial design in neurodegenerative disorders. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=225325 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.641459

Chicago Manual of Style (16th Edition):

McGhee, David J M. “Improving clinical trial design in neurodegenerative disorders.” 2014. Doctoral Dissertation, University of Aberdeen. Accessed October 26, 2020. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=225325 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.641459.

MLA Handbook (7th Edition):

McGhee, David J M. “Improving clinical trial design in neurodegenerative disorders.” 2014. Web. 26 Oct 2020.

Vancouver:

McGhee DJM. Improving clinical trial design in neurodegenerative disorders. [Internet] [Doctoral dissertation]. University of Aberdeen; 2014. [cited 2020 Oct 26]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=225325 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.641459.

Council of Science Editors:

McGhee DJM. Improving clinical trial design in neurodegenerative disorders. [Doctoral Dissertation]. University of Aberdeen; 2014. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=225325 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.641459


Queen Mary, University of London

8. Yeung, Wai Yin. Inference following biased coin designs in clinical trials.

Degree: PhD, 2013, Queen Mary, University of London

 Randomization schemes for two-treatment clinical trials are studied. Theoretical expressions for the power are derived under both complete randomization and Efron’s biased coin design for… (more)

Subjects/Keywords: 615.5072; Mathematics; Clinical Trials

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APA (6th Edition):

Yeung, W. Y. (2013). Inference following biased coin designs in clinical trials. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/8713 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.633493

Chicago Manual of Style (16th Edition):

Yeung, Wai Yin. “Inference following biased coin designs in clinical trials.” 2013. Doctoral Dissertation, Queen Mary, University of London. Accessed October 26, 2020. http://qmro.qmul.ac.uk/xmlui/handle/123456789/8713 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.633493.

MLA Handbook (7th Edition):

Yeung, Wai Yin. “Inference following biased coin designs in clinical trials.” 2013. Web. 26 Oct 2020.

Vancouver:

Yeung WY. Inference following biased coin designs in clinical trials. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2013. [cited 2020 Oct 26]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/8713 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.633493.

Council of Science Editors:

Yeung WY. Inference following biased coin designs in clinical trials. [Doctoral Dissertation]. Queen Mary, University of London; 2013. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/8713 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.633493


Boston University

9. Leatherman, Sarah Michelle. Adaptive methods for Bayesian time-to-event point-of-care clinical trials.

Degree: PhD, Biostatistics, 2014, Boston University

 Point-of-care clinical trials are randomized clinical trials designed to maximize pragmatic design features. The goal is to integrate research into standard care such that the… (more)

Subjects/Keywords: Biostatistics; Bayesian; Adaptive; Clinical trials

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APA (6th Edition):

Leatherman, S. M. (2014). Adaptive methods for Bayesian time-to-event point-of-care clinical trials. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/14317

Chicago Manual of Style (16th Edition):

Leatherman, Sarah Michelle. “Adaptive methods for Bayesian time-to-event point-of-care clinical trials.” 2014. Doctoral Dissertation, Boston University. Accessed October 26, 2020. http://hdl.handle.net/2144/14317.

MLA Handbook (7th Edition):

Leatherman, Sarah Michelle. “Adaptive methods for Bayesian time-to-event point-of-care clinical trials.” 2014. Web. 26 Oct 2020.

Vancouver:

Leatherman SM. Adaptive methods for Bayesian time-to-event point-of-care clinical trials. [Internet] [Doctoral dissertation]. Boston University; 2014. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/2144/14317.

Council of Science Editors:

Leatherman SM. Adaptive methods for Bayesian time-to-event point-of-care clinical trials. [Doctoral Dissertation]. Boston University; 2014. Available from: http://hdl.handle.net/2144/14317


University of Aberdeen

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

Degree: School of Medicine and Dentistry., 2011, University of Aberdeen

Subjects/Keywords: Clinical trials

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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?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=167718 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=167718&custom_att_2=simple_viewer

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 October 26, 2020. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=167718 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=167718&custom_att_2=simple_viewer.

MLA Handbook (7th Edition):

McPherson, Gladys. “The role of minimisation in treatment allocation for clinical trials.” 2011. Web. 26 Oct 2020.

Vancouver:

McPherson G. The role of minimisation in treatment allocation for clinical trials. [Internet] [Doctoral dissertation]. University of Aberdeen; 2011. [cited 2020 Oct 26]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=167718 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=167718&custom_att_2=simple_viewer.

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?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=167718 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=167718&custom_att_2=simple_viewer


University of Southern California

11. Ram Kumar, Charanya. CAFÉ (Common Application Framework Extensible) - a framework to support data capture for clinical trials.

Degree: MS, Applied Biostatistics and Epidemiology, 2012, University of Southern California

 CAFÉ (Common Application Framework Extensible) is a secure windows based application developed at the University of Southern California’s (USC) Norris Comprehensive Cancer Center to support… (more)

Subjects/Keywords: CAFE; clinical trials; framework

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APA (6th Edition):

Ram Kumar, C. (2012). CAFÉ (Common Application Framework Extensible) - a framework to support data capture for clinical trials. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/105677/rec/1198

Chicago Manual of Style (16th Edition):

Ram Kumar, Charanya. “CAFÉ (Common Application Framework Extensible) - a framework to support data capture for clinical trials.” 2012. Masters Thesis, University of Southern California. Accessed October 26, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/105677/rec/1198.

MLA Handbook (7th Edition):

Ram Kumar, Charanya. “CAFÉ (Common Application Framework Extensible) - a framework to support data capture for clinical trials.” 2012. Web. 26 Oct 2020.

Vancouver:

Ram Kumar C. CAFÉ (Common Application Framework Extensible) - a framework to support data capture for clinical trials. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2020 Oct 26]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/105677/rec/1198.

Council of Science Editors:

Ram Kumar C. CAFÉ (Common Application Framework Extensible) - a framework to support data capture for clinical trials. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/105677/rec/1198


Queens University

12. Jiang, Shan. Statistical Inference for the Treatment Effect in Cancer Clinical Trials .

Degree: Mathematics and Statistics, 2011, Queens University

 Randomized clinical trials provide the best evidence on the effect of treatment studied. There are different types of measures on the treatment effect, depending on… (more)

Subjects/Keywords: Treatment effect ; Clinical trials

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APA (6th Edition):

Jiang, S. (2011). Statistical Inference for the Treatment Effect in Cancer Clinical Trials . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6522

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):

Jiang, Shan. “Statistical Inference for the Treatment Effect in Cancer Clinical Trials .” 2011. Thesis, Queens University. Accessed October 26, 2020. http://hdl.handle.net/1974/6522.

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

MLA Handbook (7th Edition):

Jiang, Shan. “Statistical Inference for the Treatment Effect in Cancer Clinical Trials .” 2011. Web. 26 Oct 2020.

Vancouver:

Jiang S. Statistical Inference for the Treatment Effect in Cancer Clinical Trials . [Internet] [Thesis]. Queens University; 2011. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1974/6522.

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

Council of Science Editors:

Jiang S. Statistical Inference for the Treatment Effect in Cancer Clinical Trials . [Thesis]. Queens University; 2011. Available from: http://hdl.handle.net/1974/6522

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


Rutgers University

13. Kim, Marlene T., 1987-. Developing advanced rules and tools to improve in vivo QSAR models.

Degree: PhD, Computational and Integrative Biology, 2016, Rutgers University

Together oral bioavailability and hepatotoxicity determine the fate and failure of a new drug in clinical trials. A promising drug candidate that has little to… (more)

Subjects/Keywords: QSAR (Biochemistry); Clinical trials

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APA (6th Edition):

Kim, Marlene T., 1. (2016). Developing advanced rules and tools to improve in vivo QSAR models. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/49807/

Chicago Manual of Style (16th Edition):

Kim, Marlene T., 1987-. “Developing advanced rules and tools to improve in vivo QSAR models.” 2016. Doctoral Dissertation, Rutgers University. Accessed October 26, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/49807/.

MLA Handbook (7th Edition):

Kim, Marlene T., 1987-. “Developing advanced rules and tools to improve in vivo QSAR models.” 2016. Web. 26 Oct 2020.

Vancouver:

Kim, Marlene T. 1. Developing advanced rules and tools to improve in vivo QSAR models. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2020 Oct 26]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49807/.

Council of Science Editors:

Kim, Marlene T. 1. Developing advanced rules and tools to improve in vivo QSAR models. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49807/


Rutgers University

14. Chiarappa, Joseph A. Application of the negative multinomial distribution to comparative Poisson clinical trials of multiple experimental treatments versus a single control.

Degree: PhD, Statistics and Biostatistics, 2019, Rutgers University

Clinical trials that compare one or more experimental treatments to a control treatment in which event incidence (i.e. incidence of disease or an adverse event)… (more)

Subjects/Keywords: Poisson processes; Clinical trials  – Methodology

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APA (6th Edition):

Chiarappa, J. A. (2019). Application of the negative multinomial distribution to comparative Poisson clinical trials of multiple experimental treatments versus a single control. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/60090/

Chicago Manual of Style (16th Edition):

Chiarappa, Joseph A. “Application of the negative multinomial distribution to comparative Poisson clinical trials of multiple experimental treatments versus a single control.” 2019. Doctoral Dissertation, Rutgers University. Accessed October 26, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/60090/.

MLA Handbook (7th Edition):

Chiarappa, Joseph A. “Application of the negative multinomial distribution to comparative Poisson clinical trials of multiple experimental treatments versus a single control.” 2019. Web. 26 Oct 2020.

Vancouver:

Chiarappa JA. Application of the negative multinomial distribution to comparative Poisson clinical trials of multiple experimental treatments versus a single control. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2020 Oct 26]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60090/.

Council of Science Editors:

Chiarappa JA. Application of the negative multinomial distribution to comparative Poisson clinical trials of multiple experimental treatments versus a single control. [Doctoral Dissertation]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60090/


Columbia University

15. Overbey, Jessica Ryan. Statistical Issues in Platform Trials with a Shared Control Group.

Degree: 2020, Columbia University

 Platform trials evaluating multiple treatment arms against a shared control are an efficient alternative to multiple two-arm trials. Motivated by a randomized clinical trial of… (more)

Subjects/Keywords: Biometry; Clinical trials; Clinical trials – Methodology; Multiplicity (Mathematics); Error analysis (Mathematics)

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APA (6th Edition):

Overbey, J. R. (2020). Statistical Issues in Platform Trials with a Shared Control Group. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-yrrr-wq26

Chicago Manual of Style (16th Edition):

Overbey, Jessica Ryan. “Statistical Issues in Platform Trials with a Shared Control Group.” 2020. Doctoral Dissertation, Columbia University. Accessed October 26, 2020. https://doi.org/10.7916/d8-yrrr-wq26.

MLA Handbook (7th Edition):

Overbey, Jessica Ryan. “Statistical Issues in Platform Trials with a Shared Control Group.” 2020. Web. 26 Oct 2020.

Vancouver:

Overbey JR. Statistical Issues in Platform Trials with a Shared Control Group. [Internet] [Doctoral dissertation]. Columbia University; 2020. [cited 2020 Oct 26]. Available from: https://doi.org/10.7916/d8-yrrr-wq26.

Council of Science Editors:

Overbey JR. Statistical Issues in Platform Trials with a Shared Control Group. [Doctoral Dissertation]. Columbia University; 2020. Available from: https://doi.org/10.7916/d8-yrrr-wq26


University of Edinburgh

16. Valencia Cadavid, Sara Marcela. Model to study the flow and use of knowledge in outsourced knowledge intensive projects : a multi-case study of three vaccine clinical trials in Latin America (countries researched - Colombia, Brazil and Mexico).

Degree: PhD, 2018, University of Edinburgh

 This thesis offers insights from knowledge management theory to understand the flow of knowledge across the multiple actors involved in the execution of a clinical(more)

Subjects/Keywords: Latin America; clinical trials; knowledge flow; multi-organisational clinical trials; regulation

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APA (6th Edition):

Valencia Cadavid, S. M. (2018). Model to study the flow and use of knowledge in outsourced knowledge intensive projects : a multi-case study of three vaccine clinical trials in Latin America (countries researched - Colombia, Brazil and Mexico). (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/31495

Chicago Manual of Style (16th Edition):

Valencia Cadavid, Sara Marcela. “Model to study the flow and use of knowledge in outsourced knowledge intensive projects : a multi-case study of three vaccine clinical trials in Latin America (countries researched - Colombia, Brazil and Mexico).” 2018. Doctoral Dissertation, University of Edinburgh. Accessed October 26, 2020. http://hdl.handle.net/1842/31495.

MLA Handbook (7th Edition):

Valencia Cadavid, Sara Marcela. “Model to study the flow and use of knowledge in outsourced knowledge intensive projects : a multi-case study of three vaccine clinical trials in Latin America (countries researched - Colombia, Brazil and Mexico).” 2018. Web. 26 Oct 2020.

Vancouver:

Valencia Cadavid SM. Model to study the flow and use of knowledge in outsourced knowledge intensive projects : a multi-case study of three vaccine clinical trials in Latin America (countries researched - Colombia, Brazil and Mexico). [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1842/31495.

Council of Science Editors:

Valencia Cadavid SM. Model to study the flow and use of knowledge in outsourced knowledge intensive projects : a multi-case study of three vaccine clinical trials in Latin America (countries researched - Colombia, Brazil and Mexico). [Doctoral Dissertation]. University of Edinburgh; 2018. Available from: http://hdl.handle.net/1842/31495

17. Hardy, Rebecca Jane. Meta-analysis techniques in medical research : a statistical perspective.

Degree: PhD, 1995, London School of Hygiene and Tropical Medicine (University of London)

 Meta-analysis is now commonly used in medical research. However there are statistical issues relating to the subject that require investigation and some are considered here,… (more)

Subjects/Keywords: 610; Clinical trials; Multicentre trials

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

APA (6th Edition):

Hardy, R. J. (1995). Meta-analysis techniques in medical research : a statistical perspective. (Doctoral Dissertation). London School of Hygiene and Tropical Medicine (University of London). Retrieved from https://doi.org/10.17037/PUBS.00682268 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297183

Chicago Manual of Style (16th Edition):

Hardy, Rebecca Jane. “Meta-analysis techniques in medical research : a statistical perspective.” 1995. Doctoral Dissertation, London School of Hygiene and Tropical Medicine (University of London). Accessed October 26, 2020. https://doi.org/10.17037/PUBS.00682268 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297183.

MLA Handbook (7th Edition):

Hardy, Rebecca Jane. “Meta-analysis techniques in medical research : a statistical perspective.” 1995. Web. 26 Oct 2020.

Vancouver:

Hardy RJ. Meta-analysis techniques in medical research : a statistical perspective. [Internet] [Doctoral dissertation]. London School of Hygiene and Tropical Medicine (University of London); 1995. [cited 2020 Oct 26]. Available from: https://doi.org/10.17037/PUBS.00682268 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297183.

Council of Science Editors:

Hardy RJ. Meta-analysis techniques in medical research : a statistical perspective. [Doctoral Dissertation]. London School of Hygiene and Tropical Medicine (University of London); 1995. Available from: https://doi.org/10.17037/PUBS.00682268 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297183


University of Hong Kong

18. 李海光. Filing of complaints by the US Food and Drug Administration.

Degree: 2005, University of Hong Kong

Subjects/Keywords: Clinical trials - Evaluation.

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APA (6th Edition):

李海光.. (2005). Filing of complaints by the US Food and Drug Administration. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/131268

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

Chicago Manual of Style (16th Edition):

李海光.. “Filing of complaints by the US Food and Drug Administration.” 2005. Thesis, University of Hong Kong. Accessed October 26, 2020. http://hdl.handle.net/10722/131268.

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

MLA Handbook (7th Edition):

李海光.. “Filing of complaints by the US Food and Drug Administration.” 2005. Web. 26 Oct 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

李海光.. Filing of complaints by the US Food and Drug Administration. [Internet] [Thesis]. University of Hong Kong; 2005. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/10722/131268.

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

Council of Science Editors:

李海光.. Filing of complaints by the US Food and Drug Administration. [Thesis]. University of Hong Kong; 2005. Available from: http://hdl.handle.net/10722/131268

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


Vanderbilt University

19. Nagarsheth, Meera Bharat. A Critical Review of African American’s 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

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

APA (6th Edition):

Nagarsheth, M. B. (2016). A Critical Review of African American’s Recruitment in HIV/AIDS Clinical Trials: Why Sociostructural Context Matters. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12194

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):

Nagarsheth, Meera Bharat. “A Critical Review of African American’s Recruitment in HIV/AIDS Clinical Trials: Why Sociostructural Context Matters.” 2016. Thesis, Vanderbilt University. Accessed October 26, 2020. http://hdl.handle.net/1803/12194.

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

MLA Handbook (7th Edition):

Nagarsheth, Meera Bharat. “A Critical Review of African American’s Recruitment in HIV/AIDS Clinical Trials: Why Sociostructural Context Matters.” 2016. Web. 26 Oct 2020.

Vancouver:

Nagarsheth MB. A Critical Review of African American’s Recruitment in HIV/AIDS Clinical Trials: Why Sociostructural Context Matters. [Internet] [Thesis]. Vanderbilt University; 2016. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1803/12194.

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

Council of Science Editors:

Nagarsheth MB. A Critical Review of African American’s Recruitment in HIV/AIDS Clinical Trials: Why Sociostructural Context Matters. [Thesis]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/12194

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

20. Batidzirai, Jesca Mercy. Randomization in a two armed clinical trial: an overview of different randomization techniques.

Degree: Faculty of Science & Agriculture, 2011, University of Fort Hare

 Randomization is the key element of any sensible clinical trial. It is the only way we can be sure that the patients have been allocated… (more)

Subjects/Keywords: Clinical trials – Statistical methods; Biometry; Sampling (Statistics)

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APA (6th Edition):

Batidzirai, J. M. (2011). Randomization in a two armed clinical trial: an overview of different randomization techniques. (Thesis). University of Fort Hare. Retrieved from http://hdl.handle.net/10353/395

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):

Batidzirai, Jesca Mercy. “Randomization in a two armed clinical trial: an overview of different randomization techniques.” 2011. Thesis, University of Fort Hare. Accessed October 26, 2020. http://hdl.handle.net/10353/395.

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

MLA Handbook (7th Edition):

Batidzirai, Jesca Mercy. “Randomization in a two armed clinical trial: an overview of different randomization techniques.” 2011. Web. 26 Oct 2020.

Vancouver:

Batidzirai JM. Randomization in a two armed clinical trial: an overview of different randomization techniques. [Internet] [Thesis]. University of Fort Hare; 2011. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/10353/395.

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

Council of Science Editors:

Batidzirai JM. Randomization in a two armed clinical trial: an overview of different randomization techniques. [Thesis]. University of Fort Hare; 2011. Available from: http://hdl.handle.net/10353/395

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


North Carolina State University

21. Zhang, Min. Semiparametric Methods for Analysis of Randomized Clinical Trials and Arbitrarily Censored Time-to-event Data.

Degree: PhD, Statistics, 2009, North Carolina State University

 This dissertation includes two parts. In part one, using the theory of semiparametrics, we develop a general approach to improving efficiency of nferences in randomized… (more)

Subjects/Keywords: Covariate Adjustement; Semiparametrics; Survival Anaysis; Clinical Trials

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APA (6th Edition):

Zhang, M. (2009). Semiparametric Methods for Analysis of Randomized Clinical Trials and Arbitrarily Censored Time-to-event Data. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/5798

Chicago Manual of Style (16th Edition):

Zhang, Min. “Semiparametric Methods for Analysis of Randomized Clinical Trials and Arbitrarily Censored Time-to-event Data.” 2009. Doctoral Dissertation, North Carolina State University. Accessed October 26, 2020. http://www.lib.ncsu.edu/resolver/1840.16/5798.

MLA Handbook (7th Edition):

Zhang, Min. “Semiparametric Methods for Analysis of Randomized Clinical Trials and Arbitrarily Censored Time-to-event Data.” 2009. Web. 26 Oct 2020.

Vancouver:

Zhang M. Semiparametric Methods for Analysis of Randomized Clinical Trials and Arbitrarily Censored Time-to-event Data. [Internet] [Doctoral dissertation]. North Carolina State University; 2009. [cited 2020 Oct 26]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5798.

Council of Science Editors:

Zhang M. Semiparametric Methods for Analysis of Randomized Clinical Trials and Arbitrarily Censored Time-to-event Data. [Doctoral Dissertation]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5798


University of Toronto

22. Vera-Badillo, Emilio Francisco. Bias in Reporting of Randomized Clinical Trials in Oncology.

Degree: 2014, University of Toronto

Background:Bias in reporting efficacy and toxicity in clinical trials can influence treatment decisions. We evaluated the quality of reporting the primary endpoint and of toxicity… (more)

Subjects/Keywords: Bias; Oncology; Quality; Randomized Clinical Trials; 0564

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APA (6th Edition):

Vera-Badillo, E. F. (2014). Bias in Reporting of Randomized Clinical Trials in Oncology. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/67950

Chicago Manual of Style (16th Edition):

Vera-Badillo, Emilio Francisco. “Bias in Reporting of Randomized Clinical Trials in Oncology.” 2014. Masters Thesis, University of Toronto. Accessed October 26, 2020. http://hdl.handle.net/1807/67950.

MLA Handbook (7th Edition):

Vera-Badillo, Emilio Francisco. “Bias in Reporting of Randomized Clinical Trials in Oncology.” 2014. Web. 26 Oct 2020.

Vancouver:

Vera-Badillo EF. Bias in Reporting of Randomized Clinical Trials in Oncology. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1807/67950.

Council of Science Editors:

Vera-Badillo EF. Bias in Reporting of Randomized Clinical Trials in Oncology. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/67950


University of Wisconsin – Milwaukee

23. Gillespie, Debra Jean. Improving Research Participants' Understanding of Informed Consent.

Degree: PhD, Nursing, 2017, University of Wisconsin – Milwaukee

  ABSTRACT IMPROVING RESEARCH PARTICIPANTS’ UNDERSTANDING OF INFORMED CONSENT by Debra J. Gillespie The University of Wisconsin-Milwaukee, 2017 Under the Supervision of Professor Rachel Schiffman… (more)

Subjects/Keywords: Clinical Trials; Informed Consent; Understanding; Nursing

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

APA (6th Edition):

Gillespie, D. J. (2017). Improving Research Participants' Understanding of Informed Consent. (Doctoral Dissertation). University of Wisconsin – Milwaukee. Retrieved from https://dc.uwm.edu/etd/1475

Chicago Manual of Style (16th Edition):

Gillespie, Debra Jean. “Improving Research Participants' Understanding of Informed Consent.” 2017. Doctoral Dissertation, University of Wisconsin – Milwaukee. Accessed October 26, 2020. https://dc.uwm.edu/etd/1475.

MLA Handbook (7th Edition):

Gillespie, Debra Jean. “Improving Research Participants' Understanding of Informed Consent.” 2017. Web. 26 Oct 2020.

Vancouver:

Gillespie DJ. Improving Research Participants' Understanding of Informed Consent. [Internet] [Doctoral dissertation]. University of Wisconsin – Milwaukee; 2017. [cited 2020 Oct 26]. Available from: https://dc.uwm.edu/etd/1475.

Council of Science Editors:

Gillespie DJ. Improving Research Participants' Understanding of Informed Consent. [Doctoral Dissertation]. University of Wisconsin – Milwaukee; 2017. Available from: https://dc.uwm.edu/etd/1475


University of Cape Town

24. Nonyane, Molati. Determining the benefits realization management practices and processes in clinical trials.

Degree: MSc, Construction Economics and Management, 2019, University of Cape Town

 Benefits are measurable improvements that result from project outcomes. There is an emphasis in clinical trials literature that clinical trial benefits must always outweigh the… (more)

Subjects/Keywords: Benefits Realization Management; Processes; Clinical Trials; Strategy

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APA (6th Edition):

Nonyane, M. (2019). Determining the benefits realization management practices and processes in clinical trials. (Masters Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/30792

Chicago Manual of Style (16th Edition):

Nonyane, Molati. “Determining the benefits realization management practices and processes in clinical trials.” 2019. Masters Thesis, University of Cape Town. Accessed October 26, 2020. http://hdl.handle.net/11427/30792.

MLA Handbook (7th Edition):

Nonyane, Molati. “Determining the benefits realization management practices and processes in clinical trials.” 2019. Web. 26 Oct 2020.

Vancouver:

Nonyane M. Determining the benefits realization management practices and processes in clinical trials. [Internet] [Masters thesis]. University of Cape Town; 2019. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/11427/30792.

Council of Science Editors:

Nonyane M. Determining the benefits realization management practices and processes in clinical trials. [Masters Thesis]. University of Cape Town; 2019. Available from: http://hdl.handle.net/11427/30792

25. Schulz, Kenneth Fredrick. Methodological quality and bias in randomised controlled trials.

Degree: PhD, 1994, London School of Hygiene and Tropical Medicine (University of London)

 To evaluate the methodological quality of randomised trials in recently published articles and to examine the associations between methodological quality and bias, three related investigations… (more)

Subjects/Keywords: 519.5; Clinical trials

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APA (6th Edition):

Schulz, K. F. (1994). Methodological quality and bias in randomised controlled trials. (Doctoral Dissertation). London School of Hygiene and Tropical Medicine (University of London). Retrieved from https://doi.org/10.17037/PUBS.04646508 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321339

Chicago Manual of Style (16th Edition):

Schulz, Kenneth Fredrick. “Methodological quality and bias in randomised controlled trials.” 1994. Doctoral Dissertation, London School of Hygiene and Tropical Medicine (University of London). Accessed October 26, 2020. https://doi.org/10.17037/PUBS.04646508 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321339.

MLA Handbook (7th Edition):

Schulz, Kenneth Fredrick. “Methodological quality and bias in randomised controlled trials.” 1994. Web. 26 Oct 2020.

Vancouver:

Schulz KF. Methodological quality and bias in randomised controlled trials. [Internet] [Doctoral dissertation]. London School of Hygiene and Tropical Medicine (University of London); 1994. [cited 2020 Oct 26]. Available from: https://doi.org/10.17037/PUBS.04646508 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321339.

Council of Science Editors:

Schulz KF. Methodological quality and bias in randomised controlled trials. [Doctoral Dissertation]. London School of Hygiene and Tropical Medicine (University of London); 1994. Available from: https://doi.org/10.17037/PUBS.04646508 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321339


University of Bath

26. Temple, Jane Ruth. Adaptive designs for dose-finding trials.

Degree: PhD, 2012, University of Bath

 The pharmaceutical industry is currently facing an industry wide problem of high attrition rates for new compounds and rising development costs. As a result of… (more)

Subjects/Keywords: 615.19; adaptive; designs; clinical; trials; Bayesian; optimal

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APA (6th Edition):

Temple, J. R. (2012). Adaptive designs for dose-finding trials. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/adaptive-designs-for-dosefinding-trials(24e8bdc4-0b88-4450-b97f-bd395f634ea5).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564007

Chicago Manual of Style (16th Edition):

Temple, Jane Ruth. “Adaptive designs for dose-finding trials.” 2012. Doctoral Dissertation, University of Bath. Accessed October 26, 2020. https://researchportal.bath.ac.uk/en/studentthesis/adaptive-designs-for-dosefinding-trials(24e8bdc4-0b88-4450-b97f-bd395f634ea5).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564007.

MLA Handbook (7th Edition):

Temple, Jane Ruth. “Adaptive designs for dose-finding trials.” 2012. Web. 26 Oct 2020.

Vancouver:

Temple JR. Adaptive designs for dose-finding trials. [Internet] [Doctoral dissertation]. University of Bath; 2012. [cited 2020 Oct 26]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/adaptive-designs-for-dosefinding-trials(24e8bdc4-0b88-4450-b97f-bd395f634ea5).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564007.

Council of Science Editors:

Temple JR. Adaptive designs for dose-finding trials. [Doctoral Dissertation]. University of Bath; 2012. Available from: https://researchportal.bath.ac.uk/en/studentthesis/adaptive-designs-for-dosefinding-trials(24e8bdc4-0b88-4450-b97f-bd395f634ea5).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564007


University of Edinburgh

27. Ensor, Hannah Margaret. Statistical evaluation of surrogate outcomes : methodological extensions to ordinal outcomes with applications in acute stroke.

Degree: PhD, 2016, University of Edinburgh

 Background Surrogate outcomes are measures of treatment effect that can be used to predict treatment effect on the true outcome of interest. Surrogates are valued… (more)

Subjects/Keywords: 616.8; surrogate; clinical trials; methodology; ordinal

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APA (6th Edition):

Ensor, H. M. (2016). Statistical evaluation of surrogate outcomes : methodological extensions to ordinal outcomes with applications in acute stroke. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/22931

Chicago Manual of Style (16th Edition):

Ensor, Hannah Margaret. “Statistical evaluation of surrogate outcomes : methodological extensions to ordinal outcomes with applications in acute stroke.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed October 26, 2020. http://hdl.handle.net/1842/22931.

MLA Handbook (7th Edition):

Ensor, Hannah Margaret. “Statistical evaluation of surrogate outcomes : methodological extensions to ordinal outcomes with applications in acute stroke.” 2016. Web. 26 Oct 2020.

Vancouver:

Ensor HM. Statistical evaluation of surrogate outcomes : methodological extensions to ordinal outcomes with applications in acute stroke. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1842/22931.

Council of Science Editors:

Ensor HM. Statistical evaluation of surrogate outcomes : methodological extensions to ordinal outcomes with applications in acute stroke. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/22931


George Mason University

28. Parhat, Parwen. Randomization Tests for Regression Models in Clinical Trials .

Degree: 2013, George Mason University

 In this dissertation, we apply randomization tests in the context of regression models to detect treatment effects for clinical trial data. This application allows us… (more)

Subjects/Keywords: Statistics; clinical trials; Monte Carlo; randomization test

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APA (6th Edition):

Parhat, P. (2013). Randomization Tests for Regression Models in Clinical Trials . (Thesis). George Mason University. Retrieved from http://hdl.handle.net/1920/8287

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):

Parhat, Parwen. “Randomization Tests for Regression Models in Clinical Trials .” 2013. Thesis, George Mason University. Accessed October 26, 2020. http://hdl.handle.net/1920/8287.

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

MLA Handbook (7th Edition):

Parhat, Parwen. “Randomization Tests for Regression Models in Clinical Trials .” 2013. Web. 26 Oct 2020.

Vancouver:

Parhat P. Randomization Tests for Regression Models in Clinical Trials . [Internet] [Thesis]. George Mason University; 2013. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1920/8287.

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

Council of Science Editors:

Parhat P. Randomization Tests for Regression Models in Clinical Trials . [Thesis]. George Mason University; 2013. Available from: http://hdl.handle.net/1920/8287

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

29. Matías Sánchez, Lucía. Terapia de Presión Negativa frente a terapia convencional en la cicatrización de úlceras venosas de la extremidad inferior de pacientes hospitalizados : ensayo clínico aleatorizado: Negative Pressure Wound Therapy versus conventional therapy in healing of venous ulcers of lower extremity of hospitalized patients : randomized clinical trials.

Degree: Máster en Gestión Integral e Investigación de las Heridas Crónicas, 2017, Universidad de Cantabria

 La Terapia de Presión Negativa (TPN) es una técnica ampliamente aceptada, que se utiliza habitualmente para el cuidado de las heridas crónicas y complejas. Sin… (more)

Subjects/Keywords: Clinical trials

clinical trial with two parallel arms is proposed: 1) Intervention Group or Group A to which… …with its 95% confidence interval of both groups and Kaplan- Meier ". Keywords Clinical… …trials, Negative Pressure Wound Therapy, Biological Dressings, Wound Healing, Leg ulcer. Lucía… 

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APA (6th Edition):

Matías Sánchez, L. (2017). Terapia de Presión Negativa frente a terapia convencional en la cicatrización de úlceras venosas de la extremidad inferior de pacientes hospitalizados : ensayo clínico aleatorizado: Negative Pressure Wound Therapy versus conventional therapy in healing of venous ulcers of lower extremity of hospitalized patients : randomized clinical trials. (Masters Thesis). Universidad de Cantabria. Retrieved from http://hdl.handle.net/10902/12403

Chicago Manual of Style (16th Edition):

Matías Sánchez, Lucía. “Terapia de Presión Negativa frente a terapia convencional en la cicatrización de úlceras venosas de la extremidad inferior de pacientes hospitalizados : ensayo clínico aleatorizado: Negative Pressure Wound Therapy versus conventional therapy in healing of venous ulcers of lower extremity of hospitalized patients : randomized clinical trials.” 2017. Masters Thesis, Universidad de Cantabria. Accessed October 26, 2020. http://hdl.handle.net/10902/12403.

MLA Handbook (7th Edition):

Matías Sánchez, Lucía. “Terapia de Presión Negativa frente a terapia convencional en la cicatrización de úlceras venosas de la extremidad inferior de pacientes hospitalizados : ensayo clínico aleatorizado: Negative Pressure Wound Therapy versus conventional therapy in healing of venous ulcers of lower extremity of hospitalized patients : randomized clinical trials.” 2017. Web. 26 Oct 2020.

Vancouver:

Matías Sánchez L. Terapia de Presión Negativa frente a terapia convencional en la cicatrización de úlceras venosas de la extremidad inferior de pacientes hospitalizados : ensayo clínico aleatorizado: Negative Pressure Wound Therapy versus conventional therapy in healing of venous ulcers of lower extremity of hospitalized patients : randomized clinical trials. [Internet] [Masters thesis]. Universidad de Cantabria; 2017. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/10902/12403.

Council of Science Editors:

Matías Sánchez L. Terapia de Presión Negativa frente a terapia convencional en la cicatrización de úlceras venosas de la extremidad inferior de pacientes hospitalizados : ensayo clínico aleatorizado: Negative Pressure Wound Therapy versus conventional therapy in healing of venous ulcers of lower extremity of hospitalized patients : randomized clinical trials. [Masters Thesis]. Universidad de Cantabria; 2017. Available from: http://hdl.handle.net/10902/12403


University of Aberdeen

30. Ismail, Rehab Ahmed.; University of Aberdeen.Dept. of Applied Health Sciences. Development of core clinical measures for glaucoma effectiveness trials.

Degree: Dept. of Applied Health Sciences., 2016, University of Aberdeen

Subjects/Keywords: Glaucoma; Clinical trials.

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

APA (6th Edition):

Ismail, R. A. ;. U. o. A. D. o. A. H. S. (2016). Development of core clinical measures for glaucoma effectiveness trials. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=229470 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=229470&custom_att_2=simple_viewer

Chicago Manual of Style (16th Edition):

Ismail, Rehab Ahmed ; University of Aberdeen Dept of Applied Health Sciences. “Development of core clinical measures for glaucoma effectiveness trials.” 2016. Doctoral Dissertation, University of Aberdeen. Accessed October 26, 2020. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=229470 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=229470&custom_att_2=simple_viewer.

MLA Handbook (7th Edition):

Ismail, Rehab Ahmed ; University of Aberdeen Dept of Applied Health Sciences. “Development of core clinical measures for glaucoma effectiveness trials.” 2016. Web. 26 Oct 2020.

Vancouver:

Ismail RA;UoADoAHS. Development of core clinical measures for glaucoma effectiveness trials. [Internet] [Doctoral dissertation]. University of Aberdeen; 2016. [cited 2020 Oct 26]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=229470 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=229470&custom_att_2=simple_viewer.

Council of Science Editors:

Ismail RA;UoADoAHS. Development of core clinical measures for glaucoma effectiveness trials. [Doctoral Dissertation]. University of Aberdeen; 2016. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=229470 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=229470&custom_att_2=simple_viewer

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