Myotonic Dystrophy - Vascular and Cognition
Myotonic Dystrophy - Vascular and Cognition
Active, not recruiting · NCT04656210 · Registry updated 2026-05-22Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Myotonic Dystrophy - Vascular and Cognition | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Insulin Resistance, Muscular Disorders, Atrophic, Nutritional and Metabolic Diseases, diabetes mellitus, endocrine system disorder, glucose metabolism disease, glucose-galactose malabsorption, hereditary disease, hyperinsulinism, inherited neurodegenerative disorder, metabolic disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease, tauopathy | Active, not recruiting | Not stated | 2026-05-22 | NCT04656210 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| University Hospital, Lille | 194 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Hopital Roger Salengro, CHU Lille | Lille | France | 5 |