Why Clinical Trials are Important
Incredible breakthroughs in the treatment of cystic fibrosis have been achieved through clinical trials. Drugs and treatments that have added tomorrows — and make living with CF today better for thousands — are now available thanks to this research and everyone who volunteered to be a part of it. In order to keep promising new research moving forward, we need people with CF to participate in clinical trials.
Watch this video to hear Dr. David Orenstein, a pediatric pulmonologist and CF doctor at Children's Hospital in Pittsburgh, talk about why clinical trials are so important.
The Benefits of Participating in a Clinical Trial
There are many possible benefits to participating in a trial, including:
- Taking a more active role in your own health care
- Gaining access to new treatments not available to the public
- Getting expert medical care at leading health care facilities
- Helping others by contributing to medical research
- Receiving a treatment that works for you
"I've enjoyed participating in clinical trials basically because I know that they are helping the greater good. ... Participating in a clinical trial knowing that something in the future is going to be a benefit, it's a huge gift, and it's such a blessing for me to be able to do that." — Linda Bowman in Reflections on Clinical Trials
What About the Risks?
Although there are many possible benefits to participating in a clinical trial, there are also potential risks. Possible risks include:
- Experiencing side effects or adverse reactions to medications or treatments
- Receiving a treatment that doesn’t work for you
Your health and safety are always the priority. The research team will continuously monitor your health throughout the trial, whether you are receiving the drug being studied or a placebo.
If the research team notes any worsening of your health during the trial, they will notify your regular CF care team and the study sponsor to determine if it is related to the study drug. You should always contact the research team if you have any concerns during the clinical trial.
Remember: By signing an informed consent document, you are not signing a contract. You can leave a trial at any time. In addition, those who are monitoring the trial for safety — such as the principal investigator or the study medical monitor — can pull you from a study if they believe your health is declining.