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Study Design, Randomization, Placebos - 2009 (Session 6)

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Air date: Wednesday, October 28, 2009, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 167 * This only includes stats from October 2011 and forward.
Category: Bioethics
Runtime: 02:46:59
Description: Ethical and Regulatory Aspects of Clinical Research

Department of Clinical Bioethics

This course is designed to provide a historical context for research regulations and to help researchers and others working in human subject research gain insights and skills into the development of research protocols and their ethical implementation.

Objectives of the Course:

To learn the codes, declarations, and other documents that govern the ethical conduct of human subject research; review the critical elements of informed consent and their implementation in actual informed consent documents for clinical research; explore controversial issues relating to human subject research, including Phase I research, randomization, children in research, international research, etc; review the purpose if IRBs and provide IRB-like experience in reviewing research protocols; understand the experience of human subjects who have participated in research protocols.

8:30-9:15                    Ethics of Randomized Clinical Trials: Clinical Equipoise            

                                    Robert Truog, M.D.     

Professor of Anesthesiology & Medical Ethics

Harvard Medical School

 

9:15-9:25                    Discussion

 

9:25- 10:10                 Ethics of Placebo Controlled Trials  

                                    Frank Miller, Ph.D.

Department of Bioethics CC/NIH  

 

10:10- 10:20               Discussion

 

10:20- 10:35               Break

 

10:35- 11:30               Participant panel

For more information, visit
http://www.bioethics.nih.gov

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NLM Title: Study design, randomization, placebos / Robert Truog and Frank Miller.
Author: Truog, Robert.
National Institutes of Health (U.S.). Clinical Center
Publisher:
Abstract: (CIT): Ethical and Regulatory Aspects of Clinical Research Department of Clinical Bioethics This course is designed to provide a historical context for research regulations and to help researchers and others working in human subject research gain insights and skills into the development of research protocols and their ethical implementation. Objectives of the Course: To learn the codes, declarations, and other documents that govern the ethical conduct of human subject research; review the critical elements of informed consent and their implementation in actual informed consent documents for clinical research; explore controversial issues relating to human subject research, including Phase I research, randomization, children in research, international research, etc; review the purpose if IRBs and provide IRB-like experience in reviewing research protocols; understand the experience of human subjects who have participated in research protocols. Robert Truog, M.D. Harvard Frank Miller, Ph.D. Participant panel For more information, visit http://www.bioethics.nih.gov.
Subjects: Ethics, Research
Placebos
Randomized Controlled Trials as Topic--ethics
Publication Types: Lectures
Webcasts
Download: To download this event, select one of the available bitrates:
[384k]    How to download a Videocast
NLM Classification: QV 771
NLM ID: 101519005
CIT Live ID: 7869
Permanent link: https://videocast.nih.gov/launch.asp?15396

 

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