NCT02729597
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +11 more
- Locations
-
Not specified
Clinical trial condition
Myotonic Dystrophy
Explore clinical trials studying Myotonic Dystrophy. Study availability and eligibility vary by location and protocol.
107 public trials
35 recruiting studies
Myotonic Dystrophy trial results
NCT00004769
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +15 more
- Locations
-
Not specified
NCT00233519
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
- Locations
-
- University of Rochester Medical Center Rochester, New York, United States
NCT01136330
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Death, Death, Sudden, +16 more
- Locations
-
- Pitié Salpêtrière Hospital Paris, Île-de-France Region, France
NCT01421992
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disorders of Excessive Somnolence, Dyssomnias, +15 more
- Locations
-
- Institute of Readaptation in Physical Deficiency Québec, Quebec, Canada
NCT01242007
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
- Locations
-
- University Hospital of Nancy Vandœuvre-lès-Nancy, France
NCT00167609
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disorders of Excessive Somnolence, Dyssomnias, +14 more
- Locations
-
- CHU Angers, France
- CHU Bordeaux, France
- Raymond Poincaré Hospital Garches, France
- CHU Grenoble, France
Related conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities (106)
- Heredodegenerative Disorders, Nervous System (102)
- Neurodegenerative Diseases (102)
- Muscular Disorders, Atrophic (101)
- Musculoskeletal Diseases (101)
- Nervous System Diseases (101)
- Genetic Diseases, Inborn (99)
- Muscular Diseases (98)