Muscular Dystrophy Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People of any age (children, teenagers, or adults) who have been diagnosed with or are suspected to have Charcot-Marie-Tooth disease (CMT) or another inherited nerve condition
- People who have been diagnosed based on family history, clinical tests (such as nerve tests or physical exams), or genetic testing — even if no specific gene mutation has been identified yet
- Parents or guardians may give consent on behalf of children or teenagers who wish to participate
Who may not be able to join:
- People who do not have Charcot-Marie-Tooth disease or another inherited neuropathy (inherited nerve condition)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Allison Moore, Hereditary Neuropathy Foundation
Phone: 212-722-8396
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Identify the type of CMT; Disease Symptoms; Impact of symptoms on Activities of Daily Living; Associated Comorbidities
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.