NCT04035967
- Conditions
- Abnormalities, Multiple, Brain Damage, Chronic, Brain Diseases, +22 more
- Locations
-
- Sanko University Gaziantep, Şehitkamil, Turkey (Türkiye)
Clinical trial condition
Muscular Disorders, Atrophic
Explore clinical trials studying Muscular Disorders, Atrophic. Study availability and eligibility vary by location and protocol.
622 public trials
123 recruiting studies
Muscular Disorders, Atrophic trial results
NCT02760277
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- University of California Davis Davis, California, United States
- University of Florida Gainesville, Florida, United States
- Nemours Children's Hospital Orlando, Florida, United States
- Ann & Robert H. Lurie Children's Hospital Chicago, Illinois, United States
NCT02710591
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
- Locations
-
- I-Motion - Hôpital Armand Trousseau Paris, Île-de-France Region, France
- San Raffaele Hospital Milan, Italy
- Santa Creu i Sant Pau Hospital Barcelona, Spain
- UCL Institute of Child Health and Great Ormond Street Hospital London, United Kingdom
NCT02328482
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscular Diseases, +7 more
- Locations
-
- Montreal Neurological Institute, McGill University Montreal, Quebec, Canada
NCT02195999
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
- Locations
-
- Clinical and Translational Research Building Gainesville, Florida, United States
Completed
Effects of a Multiple Component Training Program on Muscles in Adults With Myotonic Dystrophy Type 1
NCT04001920
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- Groupe de recherche interdisciplinaire sur les maladies neuromusculaires Saguenay, Quebec, Canada
NCT02418338
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- Pediatric and Congenital Cardiology and Pulmonology Department, Arnaud De Villeneuve University Hospital Montpellier, France
Completed
Studying Skeletal Muscle, Heart, and Diaphragm Imaging in Boys With Duchenne Muscular Dystrophy
NCT01451281
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +9 more
- Locations
-
- National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States
Completed
Wearability, Saefty and Usability Assessment for the Upper Limb Exoskeleton BRIDGE/EMPATIA
NCT03951844
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscular Diseases, +5 more
- Locations
-
- IRCCS E. Medea - La Nostra Famiglia Bosisio Parini, LC, Italy
- Villa Beretta Costa Masnaga, LC, Italy
NCT03508947
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- Rare Disease Research, LLC. Atlanta, Georgia, United States
- UZ Gent Ghent, Belgium
- Universitaire Ziekenhuizen Leuven Leuven, Belgium
- CHR de la Citadelle Liège, Belgium