Enrolling in a clinical trial provides new hope for now and later.
A clinical trial involves research participants and follows a predefined plan or protocol to evaluate effects of a medical or behavioral intervention on health outcomes. By taking part in clinical trials, participants not only play a more active role in their own health care, but they also can access experimental treatments and help others by contributing to medical research.
- Infectious Diseases
- Internal Medicine
Types of Clinical Studies
A type of study in which people are observed or certain outcomes are measured. No attempt is made by the researcher to affect the outcome. For example, no treatment is given by the researcher.
During clinical trials, researchers learn if a new test or treatment works and is safe. Treatments studied in clinical trials might be new drugs or new combinations of drugs, new surgical procedures or devices, or new ways to use existing treatments. Find out more about the five phases of non-cancer clinical trials on ClinicalTrials.gov or the National Cancer Institute phases of cancer trials.
Medical Records Research
Medical records research involves the use of information collected from medical records. By studying the records of large groups of people over long periods of time, researchers can see how diseases progress and which treatments and surgeries work best.
Making an Informed Decision
Before deciding to participate in a study, you will be asked to review an informed consent form. This form will provide key facts about the study so that you can decide if participating is right for you. You must sign the informed consent form in order to participate in the study, though it is not a contract — you may still choose to leave the study at any time.
If you have questions when deciding to join a research study or at any time during it, ask a member of the study team. If your questions or concerns are not satisfactorily addressed, contact the study’s principal investigator, the Center for Research and Grants, or the Institutional Review Board (IRB).
Risks and Benefits
All medical research involves some level of risk to participants. Risks and benefits vary depending on the particular study. To help you make an informed decision, the study team is required to inform you of all known risks, benefits and available alternative health care options.
Disease Specific Trials
Clinical trials conducted at Vidant Health are primarily disease-specific. If you are interested in looking at a clinical trials by disease process, see the list of trials listed below or email us at ResearchNurseSpecialist@vidanthealth.com.