NCT04835298
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- Chu Reims Reims, France
Clinical trial condition
Myotonic Dystrophy Type 1 (DM1)
Explore clinical trials studying Myotonic Dystrophy Type 1 (DM1). Study availability and eligibility vary by location and protocol.
15 public trials
5 recruiting studies
Myotonic Dystrophy Type 1 (DM1) trial results
NCT03589677
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
Not specified
Active, Not Recruiting
Music Intervention for Brain-Heart Disease in Myotonic Dystrophy Type 1 (DM1)
NCT06809049
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +17 more
- Locations
-
- Children's Hospital of Eastern Ontario Ottawa, Ontario, Canada
Active, Not Recruiting
Global Study of Del-desiran for the Treatment of DM1
NCT06411288
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DM1, Dystrophy Myotonic, +21 more
- Locations
-
- Stanford University Stanford, California, United States
- University of Colorado Denver, Colorado, United States
- University of Florida Gainesville, Florida, United States
- University Research Center of South Florida Tampa, Florida, United States
Active, Not Recruiting
A Remote Physical Activity Program in the Population Suffering from Type 1 Myotonic Dystrophy
NCT05072288
- Conditions
- Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +12 more
- Locations
-
- Groupe de recherche interdisciplinaire Groupe de recherche interdisciplinaire sur les maladies neuromusculaires Jonquière, Quebec, Canada
- Université du Québec à Chicoutimi Saguenay, Quebec, Canada