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  1. Should desperate volunteers be included in randomised controlled trials?P. Allmark - 2006 - Journal of Medical Ethics 32 (9):548-553.
    Randomised controlled trials (RCTs) sometimes recruit participants who are desperate to receive the experimental treatment. This paper defends the practice against three arguements that suggest it is unethical first, desperate volunteers are not in equipoise. Second clinicians, entering patients onto trials are disavowing their therapeutic obligation to deliver the best treatment; they are following trial protocols rather than delivering individualised care. Research is not treatment; its ethical justification is different. Consent is crucial. Third, desperate volunteers do not give proper consent: (...)
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  • Making Babies: Is There a Right to Have Children?Mary Warnock - 2003 - Philosophical Quarterly 53 (213):626-628.
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  • Our right to in vitro fertilisation--its scope and limits.T. Tannsjo - 2008 - Journal of Medical Ethics 34 (11):802-806.
    There exists a derived negative right to procreative freedom, including a right to in vitro fertilisation (IVF) and to the exercise of selective techniques such as preimplantation genetic diagnosis. This is an extensive freedom, including not only the right to the exercise of a responsible parenthood, but also, in rare cases, to wrong decisions. It includes also a right for less than perfect parents to the use of IVF, and for IVF doctors to assist them, if they want and can (...)
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  • The organs crisis and the Spanish model: theoretical versus pragmatic considerations.M. Quigley, M. Brazier, R. Chadwick, M. N. Michel & D. Paredes - 2008 - Journal of Medical Ethics 34 (4):223-224.
    In the United Kingdom, the debate about how best to meet the shortfall of organs for transplantation has persisted on and off for many years. It is often presumed that the answer is simply to alter the law to a system of presumed consent. Acting perhaps on that presumption in his annual report launched in July, the Chief Medical Officer, Sir Liam Donaldson, advocated a system of organ donation based on presumed consent, the so-called “opt-out” system.1 He is calling for (...)
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  • “Hello, hello—it's English I speak!”: a qualitative exploration of patients' understanding of the science of clinical trials.M. Stead - 2005 - Journal of Medical Ethics 31 (11):664-669.
    Informed consent may be seriously compromised if patients fail to understand the experimental nature of the trial in which they are participating. Using focus groups, the authors explored how prospective trial participants interpret and understand the science of clinical trials by using patient information sheets relative to their medical condition. An opportunity was provided to hear in the patients’ own words how they interpret the information and why there is variable understanding. Respondents struggled to comprehend the meaning and purpose of (...)
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  • Richer Views of the Ethics of Reproduction. [REVIEW]Maura A. Ryan - 2012 - Hastings Center Report 32 (5):43-45.
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