Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Join the fight against CADASIL: new registry seeks volunteers

NCT ID NCT05567744

First seen Nov 01, 2025 · Last updated Jun 05, 2026 · Updated 36 times

Summary

This study creates a registry of people interested in CADASIL, a rare genetic brain disease. If you have CADASIL, are at risk, or have a loved one with it, you can join. Your name will be added to a list to be invited to future research studies. No treatment is given—this is about building a community for research.

Disclaimer Read more

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.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for CEREBRAL AUTOSOMAL DOMINANT ATERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Contacts and locations

Study contacts

  • Contact

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

Locations

  • University of Wisconsin

    RECRUITING

    Madison, Wisconsin, 53705, United States

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

    Contact

Conditions

The condition(s) this trial relates to.

cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.