What Are Clinical Trials?
Clinical trial is the scientific term for a test or study of a drug or medical device in people. Clinical trials are done to see if the drug or device is safe and effective for people to use. Doctors and other health professionals run the tests according to strict rules set by the Food and Drug Administration (FDA).
The FDA is part of the United States government. It is FDA's job to make sure medical treatments are safe and effective for people to use. FDA sets the rules to make sure that people who agree to be in the studies are treated as safely as possible.
Why Should Minorities And Women Participate In Clinical Trials?
In the past, most drug testing has been done on white men. This means that some groups, have not always been included in the tests done on drugs, such as:
- African Americans
- Hispanic Americans
- American Indians
- Asian Americans
But sometimes drugs work differently on people in these groups than on white men. So FDA wants people from many different groups included in these studies.
Points to Remember
- Clinical trials are tests of medical treatments to see if they are safe and if they work.
- Before you agree to take part in a study, you must be given complete information about the study, including possible side effects and benefits.
- You must sign a special agreement called "Informed Consent" before taking part in the study.
- You can leave the study at any time.
Informed Consent Protects Volunteers
To help you decide if you want to be a volunteer in a study, FDA requires that you be given complete information about the study before you agree to take part. This is known as informed consent. FDA requires that volunteers be told:
- that the study involves research of an unproven drug or device
- the purpose of the research
- how long the study is expected to take
- what will go on in the study and which parts of the study are experimental
- possible risks or discomforts
- possible benefits
- other procedures or treatments that you might want to consider instead of the treatment being studied
- that FDA may inspect study records, but the records will be kept confidential
- whether any medical treatments are available if you are hurt, what those treatments are, where they can be found, and who will pay for the treatment
- the person to contact with questions about the study, your rights, and injuries related to research
- being in the study is voluntary and you can quit at any time.
nformed consent information should be written so you can understand it. If you don't, be sure to ask the doctor or other medical person to explain it. Make sure you understand all of it before you agree to be in the study. Before you can participate in the trial, you must sign the informed consent form, showing that you have been given this information and understand it. The informed consent form is NOT a contract and you can leave the study at any time, for any reason.
Other Ways Volunteers Are Protected
Institutional Review Boards (IRBs)
Scientists, doctors and other people from the local community serve on IRBs to review and monitor their hospital's or research institution's medical research involving people. They monitor studies to help make sure that there is the least possible risk to volunteers and that the risks are reasonable in relation to the expected benefits. IRBs make sure volunteer selection is fair and that informed consent is done correctly.
Data Monitoring Committees
These committees are used mainly when one treatment is being compared with another and in studies where treatments are selected for patients at random. These committees are particularly important in tests of treatments for serious or life-threatening disease. These experts review information from studies to make sure they are being done in a way that is safest for the volunteers. During a study, if the committee finds that the treatment is harmful or of no benefit, it will stop the study. If there is evidence that one treatment gives a greater benefit than another, the committee stops the study and all volunteers are offered the better treatment.
FDA inspects records and various scientists, clinics, and other research sites involved in a study. To make sure volunteers are being protected and studies are being done correctly, from time to time such inspections are done in response to complaints.