Informed Consent for Clinical Trials: A Comparative Study of Standard Versus Simplified Forms
Davis, Terry C.
Holcombe, Randall F.
Berkel, Hans J.
Divers, Stephen G.
Journal of the National Cancer Institute 1998 May 6; 90(9): 668-674
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Protecting Research Participants Review of Institutional Review Boards: Management and Function, Edited by R.J. Amdur and E.A. Bankert; Institutional Review Board: Member Handbook, by R. Amdur; Study Guide for Institutional Review Board: Management and Function, by S. Kornetsky, A. Davis, and R.J. Amdur; Principles of Clinical Research, Edited by I. Di Giovanna and G. Hayes; Informed Consent in Medical Research, Edited by L. Doyal and J.S. Tobias; the Complete Guide to Informed Consent in Clinical Trials, Edited by T. Hartnett; Tuskegee's Truths: Rethinking the Tuskegee Syphilis Study, Edited by S.M. Reverby; European Neonatal Research: Consent, Ethics Committees and Law, Edited by S. Mason and C. Megone; the Ethics of Medical Research on Humans, by C. Foster; Ethical Issues in Biomedical Publication, Edited by A. Hudson Jones and F. McLellan; Fraud and Misconduct in Biomedical Research (3rd Edition), Edited by S. Lock, F. Wells, and M. Farthing; Biomedical Research Ethics: Updating International Guidel Nicholson, Richard (2002-11)
Miyaji, Naoko T.; Espinosa, E.; Zamora, P.; Gonzalez Baron, M.; Ferris, Timothy; Holcombe, Randall F.; Price, Frederic V.; Kelley, Joseph L.; Edwards, Robert P.; Annas, George J. (1994-09-22)
Cheung, Winson Y; Pond, Gregory R; Heslegrave, Ronald J; Enright, Katherine; Potanina, Larissa; Siu, Lillian L (2010-08)OBJECTIVES: To compare the quality of informed consent forms (ICF) for different trial phases, funding sources, oncology subspecialties, disease settings, and intervention modalities. METHODS: ICF for prospectively conducted ...