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  1. Can unequal be more fair? Ethics, subject allocation, and randomised clinical trials.A. L. Avins - 1998 - Journal of Medical Ethics 24 (6):401-408.
    Randomised clinical trials provide the most valid means of establishing the efficacy of clinical therapeutics. Ethical standards dictate that patients and clinicians should not consent to randomisation unless there is uncertainty about whether any of the treatment options is superior to the others ("equipoise"). However, true equipoise is rarely present; most randomised trials, therefore, present challenging ethical dilemmas. Minimising the tension between science and ethics is an obligation of investigators and clinicians. This article briefly reviews several techniques for addressing this (...)
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  • Toward a Duty to Report Clinical Trials Accurately: The Clinical Alert and Beyond.Kathleen Cranley Glass - 1994 - Journal of Law, Medicine and Ethics 22 (4):327-338.
    Advances in medicine depend not only on the generation of information but also on its dissemination. Clinically relevant data must be transmitted to the practitioners who will use it. Health care professionals in North America are aware of their ethical and legal obligations to inform patients adequately concerning interventions and treatments so that they may make informed choices about medical care. This obligation has been well described and defined by the courts and in the literature of medicine, ethics, and law. (...)
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  • Toward a Duty to Report Clinical Trials Accurately: The Clinical Alert and Beyond.Kathleen Cranley Glass - 1994 - Journal of Law, Medicine and Ethics 22 (4):327-338.
    Advances in medicine depend not only on the generation of information but also on its dissemination. Clinically relevant data must be transmitted to the practitioners who will use it. Health care professionals in North America are aware of their ethical and legal obligations to inform patients adequately concerning interventions and treatments so that they may make informed choices about medical care. This obligation has been well described and defined by the courts and in the literature of medicine, ethics, and law. (...)
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  • What's missing from current clinical trial guidelines? A framework for integrating science, ethics, and the community context.H. J. Sutherland, E. M. Meslin & J. E. Till - 1994 - Journal of Clinical Ethics 5 (4):297-303.
    The purpose of the work was to produce a framework to guide the development of meritorious clinical trial proposals. The framework consists of essential features of rigourous methodology, ethical acceptability, and a component referred to as "community context". These three domains were woven together in a checklist format under the headings of general, scientific and ethical considerations. Since texts concerning clinical trial methodology do not integrate ethics criteria and ethics guidelines do not provide detailed scientific criteria in obvious and practical (...)
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