North American Registry for Care and Research in MS - NARCRMS

  • STATUS
    Recruiting
  • participants needed
    100
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Updated on 19 February 2024

Summary

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.

Details
Condition Multiple sclerosis, Chronic Progressive Multiple Sclerosis, Relapsing-Remitting Multiple Sclerosis
Age 18years - 50years
Clinical Study IdentifierN/A
Last Modified on19 February 2024

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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