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25 - Research ethics

Published online by Cambridge University Press:  30 October 2009

Eric M. Meslin
Affiliation:
Professor Indiana University, Indianapolis
Bernard M. Dickens
Affiliation:
Faculty of Law University of Toronto
Peter A. Singer
Affiliation:
University of Toronto
A. M. Viens
Affiliation:
University of Oxford
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Summary

Dr. A is a family practitioner with a special interest in the treatment of chronic obstructive pulmonary disease. He receives a letter from the coordinator of a study to evaluate a promising new treatment for this condition. The letter invites Dr. A to submit the names of potentially eligible patients. He will be paid $100 for each name provided.

Dr. B, a psychiatrist in private practice, is approached by a pharmaceutical company to assist with a clinical trial to test the efficacy of a new drug in the treatment of acute psychosis. The study will enroll acutely psychotic patients with no history of psychosis (or of treatment with antipsychotic drugs) through physicians' offices and emergency departments. Patients enrolled in the study will be randomly assigned to receive the new medication or a placebo and will remain in hospital for eight weeks. During this time, they will not be permitted to receive antipsychotic medications other than the study drug. Informed consent will be obtained from each participant or a proxy. Patients may be withdrawn from the study if their medical condition worsens substantially.

What is research ethics?

Research involving human subjects can raise difficult and important ethical and legal questions. The field of research ethics is devoted to the systematic analysis of such questions to ensure that study participants are protected and, ultimately, that clinical research is conducted in a way that serves the needs of such participants and of society as a whole.

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Chapter
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Publisher: Cambridge University Press
Print publication year: 2008

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