The length of consent documents in oncological trials is doubled in twenty years-Reference-Cited by-同舟云学术

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The length of consent documents in oncological trials is doubled in twenty years

Published:2009-02 Issue:2 Volume:20 Page:379-385
ISSN:0923-7534
Container-title:Annals of Oncology
language:en
Short-container-title:Annals of Oncology

Author:

Berger O.,Grønberg B.H.,Sand K.,Kaasa S.,Loge J.H.

Funder

Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, St Olavs Hospital, N-7005 Trondheim, Norway

Publisher

Elsevier BV

Subject

Oncology,Hematology

Link

http://academic.oup.com/annonc/article-pdf/20/2/379/392910/mdn623.pdf

Reference26 articles.

1. Fifty years later: the significance of the Nuremberg Code;Shuster;N Engl J Med,1997

2. Informed consent in human experimentation and the physicians response;Beecher,2001

3. Patients’ experiences of intervention trials on the treatment of myocardial infarction: is it time to adjust the informed consent procedure to the patient's capacity?;Agard;Heart,2001

4. Informed consent and decision-making: patients’ experiences of the process of recruitment to phases I and II anti-cancer drug trials;Cox;Patient Educ Couns,2002

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5. Current Status of Electronic Informed Consent: Results of Web-based Survey Targeting Clinical Research Coordinators;Rinsho yakuri/Japanese Journal of Clinical Pharmacology and Therapeutics;2023-01-31

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