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Muscular Dystrophies

Clinical trial condition

Muscular Dystrophies

Explore clinical trials studying Muscular Dystrophies. Study availability and eligibility vary by location and protocol.

163 public trials 35 recruiting studies

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Muscular Dystrophies trial results

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

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Completed

Study of Morphology and Functional Magnetic Resonance Imaging (MRI) Muscle Patients With Muscular Dystrophy Type FSHD Benefiting a Physical Training Introduced.

NCT01990976

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral, Genetic Diseases, Inborn, +7 more
Locations: CHU de Grenbole Grenoble, France

CHU de Saint-Etienne Saint-Etienne, France

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Completed

Myocardial Fibrosis Progression in Duchenne and Becker Muscular Dystrophy - ACE Inhibitor Therapy Trial

NCT02432885

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscular Diseases, +6 more
Locations: Not specified

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Completed

Physical Training Introduction in Lifestyle of Facioscapulohumeral Dystrophy Patients

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

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Completed

Study of Albuterol and Oxandrolone in Patients With Facioscapulohumeral Dystrophy (FSHD)

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

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Completed

Randomized Study of Albuterol in Patients With Facioscapulohumeral Muscular Dystrophy

NCT00004685

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +13 more
Locations: Not specified

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Completed

Safety Study of Transvenous Limb Perfusion in Human Muscular Dystrophy

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

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Completed

Phase II Doubleblind Exploratory Study of GSK2402968 in Ambulant Subjects With Duchenne Muscular Dystrophy

NCT01153932

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: GSK Investigational Site Westmead, New South Wales, Australia

GSK Investigational Site Parkville, Victoria, Australia

GSK Investigational Site Ghent, Belgium

GSK Investigational Site Paris, France

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Completed

Evaluation of Limb-Girdle Muscular Dystrophy

NCT00893334

Conditions: Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +13 more
Locations: Children's National Medical Center Washington D.C., District of Columbia, United States

Carolinas Medical Center Charlotte, North Carolina, United States

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Completed

Tadalafil in Becker Muscular Dystrophy

NCT01070511

Conditions: Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +8 more
Locations: Cedars-Sinai Medical Center Los Angeles, California, United States

Cedars Sinai Medical Center Los Angeles, California, United States

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