| Informed consent. | |
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MedLine Citation:
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PMID: 20931166 Owner: NLM Status: In-Data-Review |
Abstract/OtherAbstract:
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Informed consent (IC) in clinical experimentation is a process by which a subject voluntarily and freely confirms his/her willingness to participate in a trial, after having been informed of all involved aspects. IC is a concept enough recent within medical tradition. Unquestionably, Nuremberg trials (1945-1947) influenced thought about consent in Medicine. When the idea of IC evolved, discussion for appropriate guidelines moved increasingly from a narrow focus on the physician's/researcher's obligation. IC shall be obtained in writing and documented before a subject is enrolled into clinical investigation. , Particularly in the case of medical devices, it is necessary an adequate information to the patient on possible incidents occurring following placing of devices. |
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Authors:
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D Sacchini; M Pennacchini |
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Publication Detail:
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Type: Journal Article |
Journal Detail:
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Title: La Clinica terapeutica Volume: 161 ISSN: 1972-6007 ISO Abbreviation: Clin Ter Publication Date: 2010 Jul-Aug |
Date Detail:
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Created Date: 2010-10-08 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 0372604 Medline TA: Clin Ter Country: Italy |
Other Details:
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Languages: eng Pagination: 397-9 Citation Subset: IM |
Affiliation:
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Institute of Bioethics, A. Gemelli School of Medicine, Università Cattolica del Sacro Cuore, Rome. |
Export Citation:
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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