Skip to main content
Department of Dermatology

Department of Dermatology

Clinical Trials

Deciding to Participate in a Clinical Research Study

Doctors meetingwith a trial participant

You should learn as much as possible about the clinical research studies that interest you. You should also feel comfortable discussing your questions and concerns with members of the research team. In addition, we recommend that you  talk to other people involved with your health care, such as family members, before participating in a clinical research study.

Prospective participants should understand what occurs during the research study, the type of health care they will receive, and any costs to them -- which may or may not include the cost of the product or costs associated with administering the product.

Anyone considering a clinical research study should also know the benefits and risks associated with participating.

Potential Benefits

  • Access to a treatment not yet available. This treatment may be more effective or have fewer side effects than the treatments that are currently available.
  • Treatment that may be free or low cost. Some clinical research studies may pay for part or all of your treatment, other medical care, travel, and other expenses during the study. But not all clinical research studies do this. Make sure you know exactly what you'll have to pay for BEFORE you agree to be part of a clinical research study.
  • Contributing to research that may help others in the future. Many treatments we have today are available because large numbers of people opted to participate in clinical research studies to test them.
  • The feeling that you're taking an active role in your care. Deciding to participate in a clinical research study can make some people feel as if they have more control over their situation, which can lead to a more positive outlook and better quality of life.

Other Considerations

  • Not being able to choose which treatment you get. In randomized studies, you are randomly assigned to get a specific treatment. In some studies, you may be assigned to get a placebo (sugar pill). In a randomized, double-blinded study, neither you nor your doctors know which treatment you're getting (but if the information is needed, it's available).
  • The new treatment may not work for you, even if it benefits other people in the trial. The new treatment could also be less effective than what is currently available.
  • More severe side effects than current treatments. This is more likely to happen with Phase I or Phase II studies.
  • Your health plan may not cover all the costs. Be sure to talk to both your health plan and one of the clinical research coordinators so you know exactly what you'll have to pay for BEFORE you agree to be part of a clinical research study.
  • More frequent testing and doctor visits. Because you'll be closely monitored, you may have to undergo testing more often than you would if you weren't in the study. This could mean more travel and time in the doctor's office or hospital for you.

The following link provides answers to Frequently Asked Questions about clinical research studies.

For additional information about dermatology clinical research studies, click on the links below:

Ongoing Clinical Research Studies 

Sign-up To Receive Information Regarding Future Clinical Research Studies 

 

Or contact us at:

Clinical Research Unit
3301 C Street, Suite 1400
Sacramento, CA 95816
Telephone: 916-734-1267
Fax: 916-442-5702
E-mail: dermstudies@ucdavis.edu