Informed Consent for Clinical Trials: Is Simpler Better?
نویسندگان
چکیده
منابع مشابه
More Nuanced Informed Consent Is Not Necessarily Better Informed Consent.
More Nuanced Informed Consent Is Not Necessarily Better Informed Consent Danielle Hornstein, Sharon Nakar, Sara Weinberger & Dov Greenbaum To cite this article: Danielle Hornstein, Sharon Nakar, Sara Weinberger & Dov Greenbaum (2015) More Nuanced Informed Consent Is Not Necessarily Better Informed Consent, The American Journal of Bioethics, 15:9, 51-53, DOI: 10.1080/15265161.2015.1062167 To lin...
متن کاملInformed consent for clinical trials: a review.
OBJECTIVE To identify and highlight challenges related to informed consent process for clinical trials in sub-Saharan Africa. DATA SOURCES Published original research findings and reviews in the English literature, together with anecdotal information from our current professional experiences with clinical trials. DESIGN Review of peer-reviewed articles. DATA EXTRACTION Online searches wer...
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متن کاملInformed consent and clinical trials: where is the placebo effect?
Informed consent requires researchers to provide participants with information about research that is accurate, complete, and understandable. Researchers also have an ethical obligation to ensure participants understand the investigational nature of the study. In clinical trials we argue that adequate information must include understandable descriptions of the function of placebos and their eff...
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The primary goal of the thousands of registered trials in cancer research is to extend survival. With evaluation of efficacy, safety, and tolerability, healthcare providers must ensure that the principles described in the Belmont Report are upheld and that patients are truly informed when signing a consent form. In this article, two cases are highlighted, and reasons for participating in clinic...
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ژورنال
عنوان ژورنال: JNCI: Journal of the National Cancer Institute
سال: 1998
ISSN: 0027-8874,1460-2105
DOI: 10.1093/jnci/90.9.644