AHealthyMe
-
Login Registration Sample personal Change Profile Log Out
Search AHealthyMe!  
Personalize AHealthyMe! -Sign up for our Newsletter!

Women's HealthMen's HealthHelath After 60Children's HealthPregnancyFitness & NutritionAlternative HealthLifestyle & WellnessWork & HealthIlls & ConditionsDental HealthSelf-Care CentersMedical LibraryCool ToolsMultimediaEn Español-

Blue Cross Blue Shield of Massachusetts

You are here: Home > Ills & Conditions > Hepatitis C and Clinical Trials


Hepatitis C and Clinical Trials 


By Peter Jaret
CONSUMER HEALTH INTERACTIVE

Below:
 • What are clinical trials?
 • Are there guidelines to participate in a clinical trial?
 • How are clinical trials conducted?


Existing drugs can eliminate hepatitis C in some patients, but they don’t work for everyone. For that reason, a variety of clinical trials are under way to test new and as-yet unapproved treatments for HCV infection.

What are clinical trials?

Clinical trials are the means by which new drugs and treatments are tested to determine if they work. They are the engine that drives progress in medicine. For patients who have run out of other options, clinical trials offer a last chance at a potentially effective therapy. In some cases they provide access to research treatments before they are made widely available.

But it’s important to remember that clinical trials often involve unproven therapies. There is no guarantee that the treatments under investigation will work. And there is always a chance that they may cause serious side effects. Still, by participating in clinical trials, patients help advance the science of medicine.

Are there guidelines to participate in a clinical trial?

Yes. If you or someone you know is interested in participating in a clinical trial, there are some important things to remember.

Clinical trials have specific guidelines about participation. To make sure clinical trials are safe and provide reliable scientific information, researchers carefully choose who can -- and who can't -- take part. Clinical trials include "inclusion criteria" (the requirements for participating) and "exclusion criteria" (factors that disallow people from taking part). These are usually spelled out in descriptions of clinical trials made available to the public.

Participants must be informed and give their consent. Doctors and nurses are required to explain the details of the investigation to prospective participants. They also provide an "informed consent" document, with the details of the study explained in writing. Participants are asked to sign the document. Additional information is sometimes provided during the study, as it becomes available.

Participants are always free to withdraw from a study. Even after you sign an informed consent document and join a clinical trial, you can withdraw at any time. Withdrawing can jeopardize research, however. So it’s important to learn everything you can before agreeing to join a trial.

Not everyone in a study always receives the active drug or treatment. Some studies test an active drug against a placebo. In blinded studies, neither participants nor researchers are allowed to know who is getting the real drug and who is being given the placebo. (A sealed code is used to keep track for later analysis.) Blinded studies are essential to eliminate bias in interpreting the results. Typically, if a drug appears to be working effectively, researchers will decide to "unblind" the study and offer the new treatment to everyone in the study.

How are clinical trials conducted?

Clinical studies are conducted in four phases. Phase I trials test a new drug or treatment in a small group of people to make sure it’s safe, to determine a safe dosage range, and to look at side effects. Phase II trials usually include more people and study both whether the drug is safe and whether it’s effective. Phase III trials include even more participants. They are designed to confirm a treatment’s effectiveness, monitor its side effects, and sometimes compare it to commonly used treatments. In Phase IV trials, drugs that have already been approved are studied for more information about their benefits, uses, or potential risks.

Investigational drugs are sometimes offered outside of clinical trials. The FDA allows manufacturers of investigational drugs to offer them to people who might benefit but who don’t qualify for clinical trials. "Expanded access," as it’s called, is usually offered to people with a serious or life-threatening illness. The drug must already have been shown to be safe and effective in well-controlled studies.

-- Peter Jaret is a contributing editor for Health magazine and a winner of the American Medical Association's award for medical reporting. His work has appeared in National Geographic, Newsweek, Hippocrates, and many other national magazines. He is also the author of In Self-Defense (Harcourt Brace Jovanovich), Active Living Every Day, and Heart Healthy for Life.



Further Resources

For more information about clinical trials:

National Institutes of Health

http://www.ClinicalTrials.gov

This site provides detailed information about clinical trials and has a search feature that locates on-going clinical trials.

CenterWatch

http://www.CenterWatch.com

This site includes a listing of clinical trials organized by state.



References


National Institutes of Health, An Introduction to Clinical Trials: http://www.clinicaltrials.gov

Chronic Hepatitis C: Disease Management, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)



Reviewed by Alexander Monto, MD, a hepatologist at the Veterans Administration Medical Center in San Francisco.


Our reviewers are members of Consumer Health Interactive's medical advisory board.
To learn more about our writers and editors, click here.

First published October 28, 2003
Last updated November 18, 2008
Copyright © 2003 Consumer Health Interactive


or find more on:

Back to top of page