NCT06093100
- Conditions
- Cardiomyopathies, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +16 more
- Locations
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- Vanderbilt University Medical Center Nashville, Tennessee, United States
Clinical trial condition
Muscular Dystrophies
Explore clinical trials studying Muscular Dystrophies. Study availability and eligibility vary by location and protocol.
452 public trials
90 recruiting studies
Muscular Dystrophies trial results
NCT01484678
- Conditions
- Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, +9 more
- Locations
-
- University of Florida Gainesville, Florida, United States
- Oregon Health and Science University Portland, Oregon, United States
- Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States
Recruiting
Natural History of Oculo-Pharyngeal Muscular Dystrophy (OPMD) - Israel National OPMD Registry
NCT07146256
- Conditions
- Blepharoptosis, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deglutition Disorders, +22 more
- Locations
-
- Sheba Medical Center Ramat Gan, Israel
NCT07136844
- Conditions
- Ataxia, Ataxia, Spinocerebellar, Autoimmune Diseases, +70 more
- Locations
-
- Centre de référence des maladies neuromusculaire, Centre Hospitalier Régional de la Citadelle Liège, Belgium
NCT06747884
- Conditions
- Childhood Myotonic Dystrophy, Congenital Myotonic Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +16 more
- Locations
-
- Virginia Commonwealth University Richmond, Virginia, United States
NCT06769633
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
- Locations
-
- Queen Fabiola Children's University Hospital HUDERF Brussels, Belgium
- Fondazione Serena Onlus - Azienda Ospedaliera Niguarda Ca' Granda - NeuroMuscolar Omnicenter Milan, Italy
- Ospedale Pediatrico Bambino Gesù Roma, Italy
- Policlinico Universitario Agostino Gemelli - Università Cattolica del Sacro Cuore Roma, Italy
Recruiting
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
NCT01793168
- Conditions
- 1p36 Deletion Syndrome, 3-Methylglutaconic Aciduria, Type V, 4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome, +698 more
- Locations
-
- Sanford Health Sioux Falls, South Dakota, United States
- Online Patient Enrollment System Sydney, Australia
NCT05004129
- Conditions
- Congenital Myotonic Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +10 more
- Locations
-
- Arkansas Children's Hospital Little Rock, Arkansas, United States
- University of California, Los Angeles (UCLA) Los Angeles, California, United States
- Stanford University Palo Alto, California, United States
- Lurie's Children's Hospital Chicago, Illinois, United States
Recruiting
Assessments in Patients With Muscular Pathology and in Control Subjects : The ActiLiège Next Study
NCT05982119
- Conditions
- Centronuclear Myopathy, Charcot-Marie-Tooth, Charcot-Marie-Tooth Disease, +25 more
- Locations
-
- CHR de la Citadelle Liège, Belgium
- Fakultni nemocnice v Motole Prague, Czechia
- Galaa Military Medical Complex Cairo, Egypt
- Semmelweis University 2nd Department of Paediatrics Budapest, Hungary
NCT06925269
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), Genetic Diseases, Inborn, +8 more
- Locations
-
- Red Nucleus Yardley, Pennsylvania, United States