11 - To Be or Not to Be – A Research Subject

Summary

For most people, the terms clinical trial, institutional review board, risk–benefit assessment, and informed consent make as much sense as the instruction manual for a complicated piece of technology. Indeed, most people probably do not know that when medical research is conducted to test a new medicine, there are rules and procedures the scientists must follow to ensure that the research is both scientifically sound and ethically safe. Most people do not know there are different kinds of medical studies; some are conducted on people who already have a disease or medical condition, and others are performed on healthy volunteers who want to help science find answers. Yet both types of potential research subjects have many of the same questions, the answers to which can help them decide whether to participate in the study, what their rights are, and what decisions they may have to make. This chapter reviews the basics of being a research subject – including the potential benefits and risks of making this important decision.

The Basics

Once you become a patient, it won't be long before somebody asks you to be a research subject. For example, your doctor might want to enroll you in a clinical trial of a new medication, possibly for a condition for which other drugs are available – such as high blood pressure – or for one for which there are no approved treatments yet.