The Choice to Become a Research Subject: A First-Person Perspective

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Rebecca Dresser, JD
Professor of Law
Washington University in St. Louis

Patients with serious illnesses are often invited to participate in clinical trials. After being diagnosed with advanced cancer, I became one of those patients. I had to choose between two options: a treatment regimen my doctors had recommended, or a trial evaluating different treatments for my disease. As someone who had taught and written about research ethics, and a long-time member of an Institutional Review Board, I was in some ways better prepared than many patients are to make this choice. And I knew about the important health benefits that come from research, as well as the arguments that patients have a duty to participate in research. Nevertheless, I decided not to enroll in the trial. Was this a defensible choice, or did I have a responsibility to contribute to a study that could help future patients in my situation?

This lecture was part of the 2016-2017 Bioethics Brownbag & Webinar Series, presented by the Center for Ethics.

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The Choice to Become a Research Subject: A First-Person Perspective

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