Clinical Research and Clinical Trials

  • Medical Author:
    Melissa Conrad Stöppler, MD

    Melissa Conrad Stöppler, MD, is a U.S. board-certified Anatomic Pathologist with subspecialty training in the fields of Experimental and Molecular Pathology. Dr. Stöppler's educational background includes a BA with Highest Distinction from the University of Virginia and an MD from the University of North Carolina. She completed residency training in Anatomic Pathology at Georgetown University followed by subspecialty fellowship training in molecular diagnostics and experimental pathology.

  • Medical Editor: William C. Shiel Jr., MD, FACP, FACR
    William C. Shiel Jr., MD, FACP, FACR

    William C. Shiel Jr., MD, FACP, FACR

    Dr. Shiel received a Bachelor of Science degree with honors from the University of Notre Dame. There he was involved in research in radiation biology and received the Huisking Scholarship. After graduating from St. Louis University School of Medicine, he completed his Internal Medicine residency and Rheumatology fellowship at the University of California, Irvine. He is board-certified in Internal Medicine and Rheumatology.

What are the pros and cons of participating in a clinical trial?

The benefits of clinical trials are many and range from taking an active role in the management of one's own health care, helping others by aiding the process of knowledge acquisition and development of enhanced treatments, being cared for by - or in accordance with the protocol which has been developed by - leading health care teams in a given field, and in some cases, receiving access to new treatments before they are approved. However, there are also risks, including side effects of drugs and risks of any procedures that may be performed. In some cases, clinical-trial participation may require more frequent doctor visits or hospitalizations than standard care, and you may have to travel to a study site that is farther away than your local health-care practitioner's office.

Some questions you may want to ask before participating in a clinical trial include the following:

  • What is the purpose of the trial?
  • Is a new type of treatment being tested? How does this differ from the accepted or standard therapy for my condition?
  • Has the drug or treatment ever been tested before?
  • How will participation impact my daily life and schedule? Will it be necessary to be in the hospital?
  • What are the risks and possible side effects of the treatment?
  • Who will pay for the treatments? Will I receive reimbursement or any type of compensation for my time or expenses?
  • How long is the trial expected to last?
  • How will I receive results of the trial, and how will I know if the treatment is successful?

Can a person leave a clinical trial once it has started?

An informed consent document is not a legal contract that requires participation in a study for the length of a study. A participant is free to leave a clinical trial at any time without prejudice to their ongoing medical care. They will not have access to the experimental medicine being studied if they leave the trial.

Medically Reviewed by a Doctor on 9/23/2015

Subscribe to MedicineNet's Newsletters

Get the latest health and medical information delivered direct to your inbox!

By clicking Submit, I agree to the MedicineNet's Terms & Conditions & Privacy Policy and understand that I may opt out of MedicineNet's subscriptions at any time.

VIEW PATIENT COMMENTS
  • Clinical Trials - Patient Experience

    Did you participate in clinical trials? Please describe your experience.

    Post
  • Clinical Trials - Patient Results

    Did the medication or technology used in your clinical trial prove effective? What were the results?

    Post

Health Solutions From Our Sponsors