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  1. The Use of Placebos in Randomized Clinical Trials.Robert J. Levine - 1985 - IRB: Ethics & Human Research 7 (2):1.
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  • Informed Consent: Legal Theory and Clinical Practice.Paul S. Appelbaum, Charles W. Lidz & Alan Meisel - 1987 - Oxford University Press USA.
    Written from the combined perspectives of a physician, lawyer, and social scientist, this book is the first reference work to provide a concise and practical overview of informed consent. Topics include the ethical theories and history of the principle of informed consent, all legal requirements for practitioners, and suggesions for making the interaction between doctor and patient clinically meaningful.
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  • Success in Spite of Failure: Why IRBs Falter in Reviewing Risks and Benefits.Peter C. Williams - 1984 - IRB: Ethics & Human Research 6 (3):1.
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  • Thinking Clearly about Research Risk: Implications of the Work of Benjamin Freedman.Charles Weijer - 1999 - IRB: Ethics & Human Research 21 (6):1.
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  • Commentary: The Randomized Clinical Trial: For Whose Benefit?Arthur Schafer - 1985 - IRB: Ethics & Human Research 7 (2):4.
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  • Placebo Orthodoxy in Clinical Research II: Ethical, Legal, and Regulatory Myths.Benjamin Freedman, Kathleen Cranley Glass & Charles Weijer - 1996 - Journal of Law, Medicine and Ethics 24 (3):252-259.
    Placebo-controlled trials are held by many, including regulators at agencies like the United States Food and Drug Administration, 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 (...)
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  • Placebo Orthodoxy in Clinical Research I: Empirical and Methodological Myths.Benjamin Freedman, Charles Weijer & Kathleen Cranley Glass - 1996 - Journal of Law, Medicine and Ethics 24 (3):243-251.
    The use of statistics in medical research has been compared to a religion: it has its high priests, supplicants, and orthodoxy. Although the comparison may be more unfair to religion than to research, a useful lesson can nonetheless be drawn: the practice of clinical research may benefit—as does the spirit—from critical self-examination. Arguably, no aspect of the conduct of clinical trials is currently more controversial—and thus in as dire need of critical examination—than the use of placebo controls. The ethical and (...)
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