NCT02729597
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +11 more
- Locations
-
Not specified
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
Completed
Electrical Impedance Myography and Ultrasound as Biomarkers of Duchenne Muscular Dystrophy
NCT01491555
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- Children's Hospital Boston Boston, Massachusetts, United States
NCT01921374
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +8 more
- Locations
-
- University Federal of São Paulo São Paulo, Brazil
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
NCT00773227
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deglutition Disorders, Digestive System Diseases, +12 more
- Locations
-
- Hospital Tenon Paris, France
NCT01027884
- Conditions
- Ambulatory Care, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +13 more
- Locations
-
- University of California Davis Medical Center Sacramento, California, United States
- Children's Hospital Colorado Aurora, Colorado, United States
- University of Florida Gainesville, Florida, United States
- Carolinas Medical Center, Neurosciences and Spine Institute Charlotte, North Carolina, United States
NCT00844597
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- Great Ormond Street Hospital London, England, United Kingdom
- Royal Victoria Infirmary Newcastle upon Tyne, England, United Kingdom
Completed
Deflazacort in Dysferlinopathies
NCT00527228
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dysferlinopathy, Genetic Diseases, Inborn, +10 more
- Locations
-
- Friedrich-Baur-Institute, Dept. of Neurology, Ludwig-Maximilians-University of Munich Munich, Germany
Completed
Modified Diet Trial: A Study of SMT C1100 in Paediatric Patients With DMD Who Follow a Balanced Diet
NCT02383511
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
- Locations
-
- Heart of England NHS Foundation Trust - Heart Lands Hospital Birmingham, United Kingdom
- Alder Hey Children's NHS Foundation Trust Liverpool, United Kingdom
- Great Ormond Street Hospital for Children NHS Foundation Trust London, United Kingdom
- Central Manchester University Hospitals NHS Foundation Trust- Royal Manchester Children's Hospital Manchester, United Kingdom
NCT02516085
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
Not specified