Myotonic Dystrophy, Congenital
Myotonic Dystrophy, Congenital
Explore linked clinical trials. Standard reference: MESH:M03356233 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Music Intervention for Brain-Heart Disease in Myotonic Dystrophy Type 1 (DM1) | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Muscular Disorders, Atrophic, Myotonic Dystrophy, Congenital, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic dystrophy type 1, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease | Active, not recruiting | Not applicable | 2026-07-28 | NCT06809049 | |
| The Spanish National Registry for Myotonic Dystrophy Type 1 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, Myotonic Dystrophy, Congenital, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic dystrophy type 1, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease | Recruiting | Not stated | 2026-02-04 | NCT07385443 | |
| Myotonic Dystrophy Family Registry | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, Myotonic Dystrophy 2, Myotonic Dystrophy, Congenital, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease | Recruiting | Not stated | 2024-11-21 | NCT02398786 |