Peripheral Neuropathy Hereditary

1

Review clinical trials related to Peripheral Neuropathy Hereditary. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Physical Activity Level at Home in CMT1A Patients: Wearable Sensor Assessment

Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common hereditary peripheral neuropathy, affecting approximately 26,000 patients in France. It presents as chronic and progressive sensorimotor deficits predominantly affecting the distal lower limbs, with onset typically in childhood. There is currently no specific pharmacological treatment; management remains symptomatic. This research will: In the long run, validated wearable sensors could improve patient follow-up, personalize rehabilitation, and support the design of clinical trials for CMT1A - including trials of the novel "Nano-Cur" treatment currently under development.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, LimogesUpdated: May 22, 2026Locations: 1
Eligibility criteria

Age ≥ 18 years [+5]

Other associated neurological condition that could independently affect walking... [+5]