Informed Consent for Alzheimer's Disease Clinical Trials: A Survey of Clinical Investigators

, , , , , &
IRB: Ethics & Human Research 24 (5):1 (2002)
  Copy   BIBTEX

Abstract

This article has no associated abstract. (fix it)

Categories

Keywords

Reprint years

DOI

10.2307/3563802

Other Versions

No versions found

Links

PhilArchive



    Upload a copy of this work     Papers currently archived: 97,197

External links

Setup an account with your affiliations in order to access resources via your University's proxy server

Through your library

My notes

Similar books and articles

Informed Consent: Practices and Views of Investigators in a Multinational Clinical Trial.Lindsay Sabik, Christine A. Pace, Heidi P. Forster-Gertner, David Wendler, Judith D. Bebchuk, Jorge A. Tavel, Laura A. McNay, Jack Killen, Ezekiel J. Emanuel & Christine Grady - 2004 - IRB: Ethics & Human Research 27 (5):13-18.
Competing Clinical Trials in the Same Institution: Ethical Issues in Subject Selection and Informed Consent.Elisa J. Gordon & Kenneth C. Micetich - 2002 - IRB: Ethics & Human Research 24 (2):1.
The quality of informed consent in a clinical research study in Thailand.Christine Pace, Ezekiel J. Emanuel, Theshinee Chuenyam, Chris Duncombe, Judith D. Bebchuk, David Wendler, Jorge A. Tavel, Laura A. McNay, Praphan Phanuphak & Heidi P. Forster - 2004 - IRB: Ethics & Human Research 27 (1):9-17.
Voluntariness of consent to research: a preliminary empirical investigation.P. S. Appelbaum, C. W. Lidz & R. Klitzman - 2008 - IRB: Ethics & Human Research 31 (6):10-14.
Ethical and regulatory aspects of clinical research: readings and commentary.Ezekiel J. Emanuel (ed.) - 2003 - Baltimore: Johns Hopkins University Press.
Ethical Issues in Cancer Chemoprevention Trials: Considerations for IRBs and Investigators.Julia Slutsman, David Buchanan & Christine Grady - 2007 - IRB: Ethics & Human Research 29 (2):1-6.
Source Data Verification in Clinical Trials Involving the Temporarily Incapacitated Subject: Is There a Missing Link in the Notion of Proxy Consent?John R. Wilson - 1992 - IRB: Ethics & Human Research 14 (4):8.
Who Understands? A Survey of 25 Words or Phrases Commonly Used in Proposed Clinical Research Consent Forms.William C. Waggoner & Diane M. Mayo - 1995 - IRB: Ethics & Human Research 17 (1):6.
Informed Consent Document and Process in India: Ethical and Quality Issues.Madhuri Patel, Kannan Sridharan & Jayesh Patel - 2016 - Asian Bioethics Review 8 (1):37-52.
Who Understands? II: A Survey of 27 Words, Phrases, or Symbols Used in Proposed Clinical Research Consent Forms.William C. Waggoner & Barbara B. Sherman - 1996 - IRB: Ethics & Human Research 18 (3):8.

Analytics

Added to PP
2021-04-28

Downloads
19 (#926,676)

6 months
12 (#445,147)

Historical graph of downloads
How can I increase my downloads?

Citations of this work

Add more citations

References found in this work

No references found.

Add more references