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You searched for subject:(clinical trials). Showing records 1 – 30 of 526 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 September 16, 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. 16 Sep 2019.

Vancouver:

Saeed I. Comparison of Methods for Handling Missing Outcome Data in Randomized Controlled Trials. [Internet] [Thesis]. Brown University; 2017. [cited 2019 Sep 16]. 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 (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 September 16, 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. 16 Sep 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 Sep 16]. 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: 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 September 16, 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. 16 Sep 2019.

Vancouver:

McPherson G. The role of minimisation in treatment allocation for clinical trials. [Internet] [Doctoral dissertation]. University of Aberdeen; 2011. [cited 2019 Sep 16]. 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. 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 September 16, 2019. 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. 16 Sep 2019.

Vancouver:

McGhee DJM. Improving clinical trial design in neurodegenerative disorders. [Internet] [Doctoral dissertation]. University of Aberdeen; 2014. [cited 2019 Sep 16]. 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


University of Hong Kong

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

Degree: MPH, 2007, University of Hong Kong

published_or_final_version

Community Medicine

Master

Master of Public Health

Subjects/Keywords: Clinical trials.

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APA (6th Edition):

鄭潤钏.; Teh, J. (2007). Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP. (Masters Thesis). University of Hong Kong. Retrieved from Teh, J. [鄭潤钏]. (2007). Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3972460 ; http://dx.doi.org/10.5353/th_b3972460 ; http://hdl.handle.net/10722/50768

Chicago Manual of Style (16th Edition):

鄭潤钏.; Teh, Jun-chuan. “Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP.” 2007. Masters Thesis, University of Hong Kong. Accessed September 16, 2019. Teh, J. [鄭潤钏]. (2007). Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3972460 ; http://dx.doi.org/10.5353/th_b3972460 ; http://hdl.handle.net/10722/50768.

MLA Handbook (7th Edition):

鄭潤钏.; Teh, Jun-chuan. “Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP.” 2007. Web. 16 Sep 2019.

Vancouver:

鄭潤钏.; Teh J. Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP. [Internet] [Masters thesis]. University of Hong Kong; 2007. [cited 2019 Sep 16]. Available from: Teh, J. [鄭潤钏]. (2007). Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3972460 ; http://dx.doi.org/10.5353/th_b3972460 ; http://hdl.handle.net/10722/50768.

Council of Science Editors:

鄭潤钏.; Teh J. Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP. [Masters Thesis]. University of Hong Kong; 2007. Available from: Teh, J. [鄭潤钏]. (2007). Globalisation of sponsored clinical trials ten years after the introduction of ICH GCP. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3972460 ; http://dx.doi.org/10.5353/th_b3972460 ; http://hdl.handle.net/10722/50768


University of Hong Kong

6. 徐佳静; Xu, Jiajing. Two-stage adaptive designs in early phase clinical trials.

Degree: M. Phil., 2013, University of Hong Kong

The primary goal of clinical trials is to collect enough scientific evidence for a new intervention. Despite the widespread use of equal randomization in clinical(more)

Subjects/Keywords: Clinical trials - Statistical methods

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APA (6th Edition):

徐佳静; Xu, J. (2013). Two-stage adaptive designs in early phase clinical trials. (Masters Thesis). University of Hong Kong. Retrieved from Xu, J. [徐佳静]. (2013). Two-stage adaptive designs in early phase clinical trials. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5089947 ; http://dx.doi.org/10.5353/th_b5089947 ; http://hdl.handle.net/10722/202252

Chicago Manual of Style (16th Edition):

徐佳静; Xu, Jiajing. “Two-stage adaptive designs in early phase clinical trials.” 2013. Masters Thesis, University of Hong Kong. Accessed September 16, 2019. Xu, J. [徐佳静]. (2013). Two-stage adaptive designs in early phase clinical trials. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5089947 ; http://dx.doi.org/10.5353/th_b5089947 ; http://hdl.handle.net/10722/202252.

MLA Handbook (7th Edition):

徐佳静; Xu, Jiajing. “Two-stage adaptive designs in early phase clinical trials.” 2013. Web. 16 Sep 2019.

Vancouver:

徐佳静; Xu J. Two-stage adaptive designs in early phase clinical trials. [Internet] [Masters thesis]. University of Hong Kong; 2013. [cited 2019 Sep 16]. Available from: Xu, J. [徐佳静]. (2013). Two-stage adaptive designs in early phase clinical trials. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5089947 ; http://dx.doi.org/10.5353/th_b5089947 ; http://hdl.handle.net/10722/202252.

Council of Science Editors:

徐佳静; Xu J. Two-stage adaptive designs in early phase clinical trials. [Masters Thesis]. University of Hong Kong; 2013. Available from: Xu, J. [徐佳静]. (2013). Two-stage adaptive designs in early phase clinical trials. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5089947 ; http://dx.doi.org/10.5353/th_b5089947 ; http://hdl.handle.net/10722/202252


Boston University

7. 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 September 16, 2019. 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. 16 Sep 2019.

Vancouver:

Leatherman SM. Adaptive methods for Bayesian time-to-event point-of-care clinical trials. [Internet] [Doctoral dissertation]. Boston University; 2014. [cited 2019 Sep 16]. 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

8. 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 (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://digitool2.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 September 16, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=167718 ; http://digitool2.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. 16 Sep 2019.

Vancouver:

McPherson G. The role of minimisation in treatment allocation for clinical trials. [Internet] [Doctoral dissertation]. University of Aberdeen; 2011. [cited 2019 Sep 16]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=167718 ; http://digitool2.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://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=167718&custom_att_2=simple_viewer


University of Wollongong

9. 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 September 16, 2019. 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. 16 Sep 2019.

Vancouver:

Jameson MG. Hitting the target: analysis of delineation and dosimetric uncertainty in radiotherapy. [Internet] [Doctoral dissertation]. University of Wollongong; 2015. [cited 2019 Sep 16]. 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 Southern California

10. 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/1196

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 September 16, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/105677/rec/1196.

MLA Handbook (7th Edition):

Ram Kumar, Charanya. “CAFÉ (Common Application Framework Extensible) - a framework to support data capture for clinical trials.” 2012. Web. 16 Sep 2019.

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 2019 Sep 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/105677/rec/1196.

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/1196


Rutgers University

11. 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 September 16, 2019. 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. 16 Sep 2019.

Vancouver:

Kim, Marlene T. 1. Developing advanced rules and tools to improve in vivo QSAR models. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2019 Sep 16]. 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/


Queen Mary, University of London

12. 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 September 16, 2019. 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. 16 Sep 2019.

Vancouver:

Yeung WY. Inference following biased coin designs in clinical trials. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2013. [cited 2019 Sep 16]. 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


Queens University

13. 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 September 16, 2019. 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. 16 Sep 2019.

Vancouver:

Jiang S. Statistical Inference for the Treatment Effect in Cancer Clinical Trials . [Internet] [Thesis]. Queens University; 2011. [cited 2019 Sep 16]. 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

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 September 16, 2019. 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. 16 Sep 2019.

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 2019 Sep 16]. 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/


Rutgers University

15. Small, Ellie, 1962-. Precision networks and information retrieval for designing and analyzing clinical studies.

Degree: PhD, Statistics, 2019, Rutgers University

A Bayesian network is a probabilistic graphical model that represents a set of variables and their conditional dependencies via one directed acyclic graph. For example,… (more)

Subjects/Keywords: Statistics and Biostatistics; Clinical trials

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

APA (6th Edition):

Small, Ellie, 1. (2019). Precision networks and information retrieval for designing and analyzing clinical studies. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/61070/

Chicago Manual of Style (16th Edition):

Small, Ellie, 1962-. “Precision networks and information retrieval for designing and analyzing clinical studies.” 2019. Doctoral Dissertation, Rutgers University. Accessed September 16, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/61070/.

MLA Handbook (7th Edition):

Small, Ellie, 1962-. “Precision networks and information retrieval for designing and analyzing clinical studies.” 2019. Web. 16 Sep 2019.

Vancouver:

Small, Ellie 1. Precision networks and information retrieval for designing and analyzing clinical studies. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2019 Sep 16]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/61070/.

Council of Science Editors:

Small, Ellie 1. Precision networks and information retrieval for designing and analyzing clinical studies. [Doctoral Dissertation]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/61070/


University of KwaZulu-Natal

16. [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.

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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 September 16, 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. 16 Sep 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 Sep 16]. 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 Edinburgh

17. 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 September 16, 2019. 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. 16 Sep 2019.

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 2019 Sep 16]. 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

18. 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 http://researchonline.lshtm.ac.uk/682268/ ; http://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 September 16, 2019. http://researchonline.lshtm.ac.uk/682268/ ; http://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. 16 Sep 2019.

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 2019 Sep 16]. Available from: http://researchonline.lshtm.ac.uk/682268/ ; http://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: http://researchonline.lshtm.ac.uk/682268/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297183


University of KwaZulu-Natal

19. Ditmore, Melissa. How ethical is your clinical trial?.

Degree: 2010, University of KwaZulu-Natal

 Is Institutional Review Board (IRB) approval and a rigorous informed consent process enough? It is our view that this is no longer the case. Conventional… (more)

Subjects/Keywords: Clinical trials – Moral and ethical aspects.

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

APA (6th Edition):

Ditmore, M. (2010). How ethical is your clinical trial?. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/8032

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):

Ditmore, Melissa. “How ethical is your clinical trial?.” 2010. Thesis, University of KwaZulu-Natal. Accessed September 16, 2019. http://hdl.handle.net/10413/8032.

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

MLA Handbook (7th Edition):

Ditmore, Melissa. “How ethical is your clinical trial?.” 2010. Web. 16 Sep 2019.

Vancouver:

Ditmore M. How ethical is your clinical trial?. [Internet] [Thesis]. University of KwaZulu-Natal; 2010. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/10413/8032.

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

Council of Science Editors:

Ditmore M. How ethical is your clinical trial?. [Thesis]. University of KwaZulu-Natal; 2010. Available from: http://hdl.handle.net/10413/8032

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


The Ohio State University

20. Mandrekar, Jayawant Narayan. Impact of change in level of risk factor(s) and proportion of cured/immune individuals on the population attributable risk : simulation based study.

Degree: PhD, Graduate School, 2002, The Ohio State University

Subjects/Keywords: Biology; Clinical trials

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APA (6th Edition):

Mandrekar, J. N. (2002). Impact of change in level of risk factor(s) and proportion of cured/immune individuals on the population attributable risk : simulation based study. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1486462067843814

Chicago Manual of Style (16th Edition):

Mandrekar, Jayawant Narayan. “Impact of change in level of risk factor(s) and proportion of cured/immune individuals on the population attributable risk : simulation based study.” 2002. Doctoral Dissertation, The Ohio State University. Accessed September 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1486462067843814.

MLA Handbook (7th Edition):

Mandrekar, Jayawant Narayan. “Impact of change in level of risk factor(s) and proportion of cured/immune individuals on the population attributable risk : simulation based study.” 2002. Web. 16 Sep 2019.

Vancouver:

Mandrekar JN. Impact of change in level of risk factor(s) and proportion of cured/immune individuals on the population attributable risk : simulation based study. [Internet] [Doctoral dissertation]. The Ohio State University; 2002. [cited 2019 Sep 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486462067843814.

Council of Science Editors:

Mandrekar JN. Impact of change in level of risk factor(s) and proportion of cured/immune individuals on the population attributable risk : simulation based study. [Doctoral Dissertation]. The Ohio State University; 2002. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486462067843814

21. 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 http://researchonline.lshtm.ac.uk/4646508/ ; http://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 September 16, 2019. http://researchonline.lshtm.ac.uk/4646508/ ; http://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. 16 Sep 2019.

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 2019 Sep 16]. Available from: http://researchonline.lshtm.ac.uk/4646508/ ; http://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: http://researchonline.lshtm.ac.uk/4646508/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321339


University of KwaZulu-Natal

22. [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.

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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 September 16, 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. 16 Sep 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 Sep 16]. 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


University of KwaZulu-Natal

23. [No author]. How ethical is your clinical trial? .

Degree: 2010, University of KwaZulu-Natal

 Is Institutional Review Board (IRB) approval and a rigorous informed consent process enough? It is our view that this is no longer the case. Conventional… (more)

Subjects/Keywords: Clinical trials – Moral and ethical aspects.

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APA (6th Edition):

author], [. (2010). How ethical is your clinical trial? . (Thesis). University of KwaZulu-Natal. Retrieved from http://dx.doi.org/10.1111/j.1742-1241.2010.02421.x

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. “How ethical is your clinical trial? .” 2010. Thesis, University of KwaZulu-Natal. Accessed September 16, 2019. http://dx.doi.org/10.1111/j.1742-1241.2010.02421.x.

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. “How ethical is your clinical trial? .” 2010. Web. 16 Sep 2019.

Vancouver:

author] [. How ethical is your clinical trial? . [Internet] [Thesis]. University of KwaZulu-Natal; 2010. [cited 2019 Sep 16]. Available from: http://dx.doi.org/10.1111/j.1742-1241.2010.02421.x.

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

Council of Science Editors:

author] [. How ethical is your clinical trial? . [Thesis]. University of KwaZulu-Natal; 2010. Available from: http://dx.doi.org/10.1111/j.1742-1241.2010.02421.x

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

24. 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 September 16, 2019. 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. 16 Sep 2019.

Vancouver:

Batidzirai JM. Randomization in a two armed clinical trial: an overview of different randomization techniques. [Internet] [Thesis]. University of Fort Hare; 2011. [cited 2019 Sep 16]. 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

25. Burrett, Julie Ann. Identification of randomized trials for inclusion in meta-analyses of treatments for childhood acute lymphoblastic leukaemia, and investigation of factors leading to publication bias.

Degree: 2003, Open University

 <b>Purpose</b>: Some randomized trials are reported widely, while others remain unpublished. It is essential to systematic reviewers and meta-analysts that factors leading to publication bias… (more)

Subjects/Keywords: 616.0277; Clinical trials

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APA (6th Edition):

Burrett, J. A. (2003). Identification of randomized trials for inclusion in meta-analyses of treatments for childhood acute lymphoblastic leukaemia, and investigation of factors leading to publication bias. (Doctoral Dissertation). Open University. Retrieved from http://oro.open.ac.uk/22376/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288336

Chicago Manual of Style (16th Edition):

Burrett, Julie Ann. “Identification of randomized trials for inclusion in meta-analyses of treatments for childhood acute lymphoblastic leukaemia, and investigation of factors leading to publication bias.” 2003. Doctoral Dissertation, Open University. Accessed September 16, 2019. http://oro.open.ac.uk/22376/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288336.

MLA Handbook (7th Edition):

Burrett, Julie Ann. “Identification of randomized trials for inclusion in meta-analyses of treatments for childhood acute lymphoblastic leukaemia, and investigation of factors leading to publication bias.” 2003. Web. 16 Sep 2019.

Vancouver:

Burrett JA. Identification of randomized trials for inclusion in meta-analyses of treatments for childhood acute lymphoblastic leukaemia, and investigation of factors leading to publication bias. [Internet] [Doctoral dissertation]. Open University; 2003. [cited 2019 Sep 16]. Available from: http://oro.open.ac.uk/22376/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288336.

Council of Science Editors:

Burrett JA. Identification of randomized trials for inclusion in meta-analyses of treatments for childhood acute lymphoblastic leukaemia, and investigation of factors leading to publication bias. [Doctoral Dissertation]. Open University; 2003. Available from: http://oro.open.ac.uk/22376/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.288336


University of Hong Kong

26. 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.

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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 September 16, 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. 16 Sep 2019.

Vancouver:

Li H. Filing of complaints by the US Food and Drug Administration. [Internet] [Masters thesis]. University of Hong Kong; 2005. [cited 2019 Sep 16]. 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 Louisville

27. Barnes, Christopher Noel. A phase II two stage clinical trial design to handle latent heterogeneity for a binary response.

Degree: PhD, 2010, University of Louisville

 Phase II clinical trial are generally single arm trial where a homogeneity assumption is placed on the response. In practice, this assumption may be violated… (more)

Subjects/Keywords: Phase II clinical trials; Overdispersion; Heterogeneity

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APA (6th Edition):

Barnes, C. N. (2010). A phase II two stage clinical trial design to handle latent heterogeneity for a binary response. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/71 ; https://ir.library.louisville.edu/etd/71

Chicago Manual of Style (16th Edition):

Barnes, Christopher Noel. “A phase II two stage clinical trial design to handle latent heterogeneity for a binary response.” 2010. Doctoral Dissertation, University of Louisville. Accessed September 16, 2019. 10.18297/etd/71 ; https://ir.library.louisville.edu/etd/71.

MLA Handbook (7th Edition):

Barnes, Christopher Noel. “A phase II two stage clinical trial design to handle latent heterogeneity for a binary response.” 2010. Web. 16 Sep 2019.

Vancouver:

Barnes CN. A phase II two stage clinical trial design to handle latent heterogeneity for a binary response. [Internet] [Doctoral dissertation]. University of Louisville; 2010. [cited 2019 Sep 16]. Available from: 10.18297/etd/71 ; https://ir.library.louisville.edu/etd/71.

Council of Science Editors:

Barnes CN. A phase II two stage clinical trial design to handle latent heterogeneity for a binary response. [Doctoral Dissertation]. University of Louisville; 2010. Available from: 10.18297/etd/71 ; https://ir.library.louisville.edu/etd/71


University of Aberdeen

28. 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://digitool2.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 September 16, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=229470 ; http://digitool2.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. 16 Sep 2019.

Vancouver:

Ismail RA;UoADoAHS. Development of core clinical measures for glaucoma effectiveness trials. [Internet] [Doctoral dissertation]. University of Aberdeen; 2016. [cited 2019 Sep 16]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=229470 ; http://digitool2.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://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=229470&custom_att_2=simple_viewer


University of Edinburgh

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

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 September 16, 2019. 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. 16 Sep 2019.

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 2019 Sep 16]. 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

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

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 September 16, 2019. 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. 16 Sep 2019.

Vancouver:

Parhat P. Randomization Tests for Regression Models in Clinical Trials . [Internet] [Thesis]. George Mason University; 2013. [cited 2019 Sep 16]. 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

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