Global quest to map a rare nerve disease

NCT ID NCT03920774

Summary

This study aims to learn more about familial dysautonomia, a rare inherited nerve disorder, by observing 400 patients over time. Researchers will collect health information and optional blood samples to track how the disease changes and to find better ways to measure it. The goal is to gather knowledge that will help design future treatment trials, but this study itself does not test any new treatments.

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes NO responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Email: •••••@•••••

Locations

  • Dysautonomia Center - School of Medicine -NYU Langone Medical Center

    RECRUITING

    New York, New York, 10016, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact Email: •••••@•••••

    Contact

  • Sheba Medical Center - Safra Children's Hospital

    RECRUITING

    Tel Litwinsky, Ramat Gan, 52621, Israel

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact Phone: •••-•••-•••• Email: •••••@•••••

Conditions

Explore the condition pages connected to this study.