Placebo Orthodoxy in Clinical Research II: Ethical, Legal, and Regulatory Myths

Author:

Freedman Benjamin,Glass Kathleen Cranley,Weijer Charles

Abstract

Placebo-controlled trials are held by many, including regulators at agencies like the United States Food and Drug Administration (FDA), to be the gold standard in the assessment of new medical interventions. Yet the use of placebo controls in clinical trials has been the focus of considerable controversy. In this two-part article, we challenge a number of common beliefs concerning the value of placebo controls. Part I critiques statistical and other scientific justifications for the use of placebo controls in clinical research. The continued use of placebo controls in clinical trials on diseases for which accepted treatment exists raises equally important ethical, legal, and regulatory issues for which various justifications have been given. Defense of this practice relies on normative as well as empirical myths.In their attack on the prevailing use of placebo controls, Kenneth Rothman and Karin Michels emphasize that this practice stands in violation of the World Medical Association's guidelines on the ethics of human experimentation, most commonly known as the Helsinki Declaration.

Publisher

Cambridge University Press (CUP)

Subject

Health Policy,General Medicine,Issues, ethics and legal aspects

Reference55 articles.

1. 20. National Institutes of Health, Office for Protection from Research Risks, Protecting Human Subjects: Institutional Review Board Handbook (Washington, D.C.: U.S. Government Printing Office, 1993): At 4–23.

2. 22. Halushka v. University of Saskatchewan, (1965) 93 D.L.R. 2d 436; and Kus v. Sherman Hospital, 644 N.E.2d 1214 (Ill. App. 1995).

3. 7. Medical Research Council of Canada, Guidelines on Research Involving Human Subjects (Ottawa: Minister of Supply & Services, 1987).

4. 2. Id.

5. “Ethics and Placebo-Controlled Thrombolytic Trials: The Future,”;Freedman;Coronary Artery Disease,1991

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