Clin2
NCT07156214Likely a fitRecruiting

Understanding RFC1-ataxia to find biomarkers

CANVAS Syndrome

Part of Brain & nervous system, Genetic & congenital clinical trials.

This study looks at a rare genetic condition called RFC1-ataxia (also known as CANVAS). It aims to find better ways to diagnose and track the disease. You may qualify if you have this condition, are between 18 and 80, and can agree to take part.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
50 people
Ages
18 years to 80 years
Study type
Interventional

Who can take part

  • You must have been diagnosed with RFC1-ataxia (a movement disorder caused by a specific gene change).
  • You must be between 18 and 80 years old.
  • You must be able to understand and sign a consent form agreeing to join the study.
  • You should not have any other major nerve or brain disease.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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