Making the Decision

Deciding whether or not to participate in a clinical research trial requires careful consideration. It is important that you weigh all of the pros and cons before you commit to participate.

Here are a few things to consider before you enroll:

Potential Benefits

• You will receive access to first-class medical care at no-cost to you or your insurance.
• You will have access to cutting-edge treatments that may not be available to the general public.
• You will receive one-on-one care from a team of medical experts focused on you and your specific condition.
• You will have the opportunity to learn more about your condition and how you can manage it.
• You will have the knowledge and satisfaction of knowing that you are helping others by participating in the process of finding new treatments and cures.

  Potential Drawbacks

• Study participation requires a commitment on your part to adhere to the study protocol and the instructions of the clinical investigator.
• You will need to make and keep office appointments as scheduled. Study protocols require that visits occur on a specific timeline.
• You may need to keep a logbook or diary of your symptoms. It is important that you complete the diary as required.
• The study treatment may not relieve your symptoms or improve your condition.
• Some studies include the use of a placebo or "sugar pill." It is possible that you could receive the placebo treatment.

Other Things to Consider

As a study participant, you are free to withdraw at any time; your participation is completely voluntary.

During the enrollment process, the investigator and his staff will review the study protocol, its benefits, and its risks with you. You can always decide to opt-out if you find that the study isn't right for you.

How to Learn More

If you would like to learn more about a specific study, or study participation in general, we would be happy to answer any questions you might have. Please feel free to contact us at any time at (801) 409-2040.