congenital muscular dystrophy
congenital muscular dystrophy
Explore linked clinical trials. Standard reference: MONDO:00199502 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Swiss Registry for Neuromuscular Disorders | Duchenne muscular dystrophy, congenital muscular dystrophy, proximal spinal muscular atrophy | Recruiting | Not stated | 2026-01-15 | NCT05102916 | |
| Assessments in Patients With Muscular Pathology and in Control Subjects : The ActiLiège Next Study | Charcot-Marie-Tooth disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, X-linked disease, central nervous system malformation, centronuclear myopathy, congenital muscular dystrophy, congenital structural myopathy, facioscapulohumeral muscular dystrophy, hereditary disease, hereditary motor and sensory neuropathy, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy | Recruiting | Not applicable | 2025-05-20 | NCT05982119 |