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Track this trial| NCT Number | NCT05902351 |
| Lead Sponsor | Hereditary Neuropathy Foundation |
| Conditions (from sponsor) |
Charcot-Marie-Tooth Disease, Charcot-Marie-Tooth, Charcot-Marie-Tooth Disease, Type IA, Charcot-Marie-Tooth Disease Type 2A, Charcot-Marie-Tooth Disease Type 2, Charcot-Marie-Tooth Disease, Type 2C, Charcot-Marie-Tooth Disease Type 2A2B, Charcot-Marie-Tooth Disease Type 2B2 +41 more |
| Related terms | [OBSOLETE] Charcot-Marie-Tooth disease, Type 2C, Charcot-Marie-Tooth Disease, Charcot-Marie-Tooth disease and deafness, Charcot-Marie-Tooth Disease, Axonal, Type 2a1, Charcot-Marie-Tooth Disease, Axonal, Type 2A2, Charcot-Marie-Tooth Disease, Axonal, Type 2n, Charcot-Marie-Tooth disease, Type 1C, Charcot-Marie-Tooth disease, Type 1D, Charcot-Marie-Tooth disease, Type 1F, Charcot-Marie-Tooth disease, Type 2A, Charcot-Marie-Tooth disease, Type 2B2, Charcot-Marie-Tooth disease, Type 2D, Charcot-Marie-Tooth disease, Type 2E, Charcot-Marie-Tooth disease, Type 2H, Charcot-Marie-Tooth disease, Type 2I, Charcot-Marie-Tooth disease, Type 2J, Charcot-Marie-Tooth disease, Type 2K, Charcot-Marie-Tooth disease, Type 4A, Charcot-Marie-Tooth disease, Type 4A, axonal form, Charcot-Marie-Tooth disease, Type 4B1, Charcot-Marie-Tooth disease, Type 4B2, Charcot-Marie-Tooth disease, Type 4C, Charcot-Marie-Tooth disease, Type 4E, Charcot-Marie-Tooth Disease, Type 4H, Disease, Limb-girdle muscular dystrophy, type 1B, Neuropathy, hereditary motor and sensory, LOM type, Peripheral Nervous System Diseases |
| Enrollment | 10,000 participants |
| Start Date | |
| Primary Completion | (estimated) |
| Study Completion | (estimated) |
| Updated on ClinicalTrials.gov |