Clin2
NCT01193075Possibly a fitRecruiting

Tracking the course of charcot-marie-tooth disease over time

Charcot Marie Tooth Disease

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

This study follows people with certain types of Charcot-Marie-Tooth disease (CMT), a genetic nerve disorder, over time to understand how the condition progresses. It also includes healthy volunteers as controls, and no experimental treatments are given.

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

Phase
N/A
Enrollment
5,000 people
Ages
Any age
Study type
Observational

Who can take part

  • You or a close relative must have a confirmed gene change that causes CMT (or a strongly suspected one).
  • If you don't have your own genetic test result, you need a family member with a confirmed gene change and a clear link to your condition.
  • You must not have another known cause for your nerve problems, like diabetes or injury.
  • If you're a control participant, you must not have any nerve problems.
  • You must be willing to sign a consent form (teenagers 13-17 need to sign an assent form).

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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