NCT01990976
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral, Genetic Diseases, Inborn, +7 more
- Locations
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- CHU de Grenbole Grenoble, France
- CHU de Saint-Etienne Saint-Etienne, France
Clinical trial condition
Muscular Disorders, Atrophic
Explore clinical trials studying Muscular Disorders, Atrophic. Study availability and eligibility vary by location and protocol.
628 public trials
120 recruiting studies
Muscular Disorders, Atrophic trial results
NCT00312247
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- UCLA Department of Orthopaedic Surgery Los Angeles, California, United States
- Shriners Hospitals for Children Sacramento, California, United States
- Shriners Hospitals for Children Portland, Oregon, United States
NCT02159612
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Disease Progression, +11 more
- Locations
-
- Neuromuscular Research Unit, Department of Neurology, Rigshospitalet Copenhagen, Denmark
NCT02432885
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscular Diseases, +6 more
- Locations
-
Not specified
NCT01874275
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- Alan Neuromedical Houston, Texas, United States
NCT01116570
- Conditions
- Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +8 more
- Locations
-
- CHU de Grenoble Grenoble, France
- CHU de Saint-Etienne Saint-Etienne, France
NCT00027391
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscle Weakness, +11 more
- Locations
-
- Ohio State University Medical Center Columbus, Ohio, United States
NCT00004685
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +13 more
- Locations
-
Not specified
NCT00873782
- Conditions
- Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, +11 more
- Locations
-
- University of North Carolina at Chapel Hill Chapel Hill, North Carolina, United States
NCT01645098
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- Nationwide Children's Hospital Columbus, Ohio, United States