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Clinical Trial Resources

NARCOMS Patient Registry

This registry of people willing to participate in MS research was initiated by the Consortium of MS Centers to facilitate multicenter studies. As of May 2007, the number of participants surpassed 32,000. Information is available in Spanish. Read more about Narcoms here, read NARCOMS Now magazine, or visit the website by clicking below.



Free Webinar on Clinical Trial Participation

AWARE for All is a free clinical research education program from the Center for Information and Study on Clinical Research Participation. Speakers will discuss what to expect from a clinical trial
and the importance of participating. Visit exhibits from local 
health and wellness

Learn More

Learn More


New and better therapies would not be possible without people living with MS who are willing to serve as volunteers in clinical trials. For more information, explore these other sites and resources:


A publishing and information services company that provides information on clinical trials, including a list of MS studies currently recruiting patients.


The Center for Information and Study on Clinical Research Participation educates and empowers patients, medical and research professionals, the media and policymakers about clinical research participation and what it means to be an active participant in the process. CISCRP also sponsors the Clinical Research Volunteer Community, an online community to share and learn from the experiences of those involved in clinical research.

A registry of clinical trials that are currently recruiting participants with many disorders in the United States and around the world. Searchable by disease.

NIH Clinical Trials and You

Visitors to the website will find information about: The basics of clinical trial participation, first hand experiences from actual clinical trial volunteers, explanations from researchers, and links on how to search for a trial or enroll in a research matching program. Health care professionals can read about evidence-based strategies for talking with patients about trials, print audience-tested posters to help promote trials in clinics and offices, and find other educational materials.


PatientsLikeMe has integrated its clinical trials tool with to develop a site that allows patients to find trials listed on which are recruiting participants (including studies of drugs, devices, therapy, or non-interventional studies such as genetics or questionnaires); patients can search based on condition, age, sex, location, and other criteria.

A not-for-profit secure Web site, designed to provide people who are interested in participating in research the opportunity to be matched with studies that may be the right fit for them. ResearchMatch is a collaborative effort of the national network of medical research institutions affiliated with the Clinical and Translational Science Awards, a part of the National Institutes of Health.


The Gift of Participation: A Guide to Making Informed Decisions About Volunteering for a Clinical Trial
by Ken Getz
Order through CISCRP

Human Trials: Scientists, Investors, and Patients in the Quest for a Cure
by Susan Quinn
Order through


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