NCT04999735
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscular Diseases, +6 more
- Locations
-
- Centre for Human Drug Research Leiden, South Holland, Netherlands
Clinical trial condition
Muscular Dystrophy, Facioscapulohumeral
Explore clinical trials studying Muscular Dystrophy, Facioscapulohumeral. Study availability and eligibility vary by location and protocol.
15 public trials
6 recruiting studies
Muscular Dystrophy, Facioscapulohumeral trial results
Completed
Evaluation of a Textile Scapula Orthosis
NCT04154098
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscle Weakness, +15 more
- Locations
-
- Kliniken Schmieder Konstanz Konstanz, Basen-Wuerttemberg, Germany
- ETH Zurich Zurich, Switzerland
NCT01689480
- Conditions
- Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +8 more
- Locations
-
- CHU de Grenbole Grenoble, France
- CHU de Saint-Etienne Saint-Etienne, France
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
NCT00004685
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +13 more
- Locations
-
Not specified