North American Registry for Care and Research in MS - NARCRMS
NARCRMS is a national database that collects patient and physician-based information on MS and will bring together information and data collected in multiple registries and databases across the U.S. and Canada. We expect that data collected consistently over long periods of time, when carefully studied, will 1) produce new clues to the causes of MS, 2) significantly enhance the ability of physicians, other clinicians, and patients to manage symptoms, and 3) potentially affect the progression of the disorder, and perhaps lead to the eventual eradication of MS.
- Study Identifier: 823894
Contact the research team to learn more about this study.
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