A clinical trial is a clinical research study where participants receive specific interventions — such as a drug, a device, a new screening test, a behavior change or procedure or other alternative therapy — under close medical monitoring and according to the research plan or protocol created by the investigators (often medical doctors). A clinical study involves research that is intended to add to medical knowledge related to the treatment, diagnosis and prevention of diseases or conditions. Without clinical trials, we would not be able to move medicine forward.
Be sure to consult with your physician before participating in a clinical trial.
Throughout our health system, researchers and medical experts are conducting a variety of clinical trials:
Clinical research studies are designed to answer specific medical questions. Some clinical research studies test new drugs or new combinations of drugs, new surgical procedures or devices or new ways to use existing treatments. Other research studies might involve long-term observation of patients to better understand how health or diseases progress. The goal of clinical research is to discover better ways to treat, prevent, diagnose or understand human disease.
Both healthy patients and patients with an illness or disease can volunteer to be in a clinical trial. FMOL Health offers clinical trials for adult and pediatric patients in several of the regions we serve. Patients who decide to participate in a research study usually must complete the informed consent process before they participate in the clinical trial.
During the informed consent process, patients are provided with the information they need to make their decision about participating in a clinical trial. Members of the research team meet with the patient and provide them with an informed consent form that explains the details of the study, including the purpose, duration, required procedures, potential risks and benefits, and contact information for the research team. Patients are given time to ask questions, consult with their family, or talk to their doctors before they sign the informed consent document. Participating in a clinical trial is voluntary. Patients can refuse to participate or can withdraw from the study at any time without the loss of any medical benefit to which the patient is entitled.
You can sign up for a clinical trial by:
If you are a patient at an FMOL Health hospital or clinic, you may be asked to participate in a research study.
Clinical trials are funded by different sources, including pharmaceutical companies, device companies, the National Institutes of Health or other sponsors. FMOL Health is committed to ensuring that financial interests or other conflicts of interest do not compromise the protection of research subjects or the integrity of the research findings.