The Physician/Investigator's Obligation to Patients Participating in Research: The Case of Placebo Controlled Trials

Author:

Glass Kathleen Cranley,Waring Duff

Abstract

Some authors argue that the ethics of medical care and the ethics of research differ, and that it is a mistake to conflate the two. They propose “that medical research and medical treatment are two distinct forms of activities, governed by different ethical principles.” This raises the question of whether physicians who are also clinical investigators may separate their role as physician from that of researcher when they are involved in clinical trials, thereby avoiding the obligations required in the physician-patient relationship. Miller and Brody suggest that medical training is to blame for what they believe is the physicians’ tendency to confound the obligations of research and practice. “Physician-investigators, after all, went to medical school” they explain. They believe that considering research with patients outside the ethical framework of the physician-patient relationship may be “difficult and threatening” to physicians who have “psychological needs” to consider the ethical obligations flowing from their relationship with their patients.

Publisher

Cambridge University Press (CUP)

Subject

Health Policy,General Medicine,Issues, ethics and legal aspects

Reference82 articles.

1. 22 Crits v. Sylvester, 1 D.L.R. (2d.) 502, 508, (1956), aff'd [1956] S.C.R. 991.

2. 64 Id; Temple, Ellenberg, , supra note 5.

3. The Rise of Litigation in Human Subjects Research

4. 40 Lockett v. Goodill, 430 P.2d 589, 591 (WA, 1967), as cited by Hall, Bobinski, Orenticher, , supra note 35.

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