Study of the natural course of Charcot-Marie-Tooth disease
Part of Brain & nervous system, Genetic & congenital clinical trials.
This study looks at how Charcot-Marie-Tooth disease (CMT) or related inherited nerve conditions change over time. It may help researchers better understand what to expect and guide future treatments.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have Charcot-Marie-Tooth disease (CMT) or another inherited neuropathy
- You can confirm the diagnosis (from a doctor exam, nerve tests, family history, and/or genetic testing) or be suspected of it
- If you’re a child or teen, a parent or guardian agrees and signs consent
- You agree to participate by reviewing and signing the consent form electronically
- If you do not have CMT or a related inherited nerve condition, you cannot join
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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