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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.

165 public trials 36 recruiting studies

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Muscular Dystrophies trial results

Completed

Ultrasound in Muscle Biopsy

NCT01790178

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscular Diseases, +8 more
Locations: Duke University Medical Center Durham, North Carolina, United States

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Completed

ECoG Direct Brain Interface for Individuals With Upper Limb Paralysis

NCT01393444

Conditions: ALS, Brachial Plexus Injury, Brain Diseases, +33 more
Locations: University of Pittsburgh Pittsburgh, Pennsylvania, United States

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Completed

Muscle MRI in Becker Muscular Dystrophy and in Limb-girdle Muscular Dystrophy Type 2I

NCT02165358

Conditions: Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +10 more
Locations: Neuromuscular Research Unit, Rigshospitalet Copenhagen, Denmark

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Completed

Quality of Life in Neuromuscular Disease

NCT02895763

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscular Diseases, +6 more
Locations: Chu de Reims Reims, France

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Completed

Prospective Study for 24-months of Physical Training Introduced in Lifestyle of Patients With FSHD : Tolerance, Sustainability and Efficiency of Unsupervised Training Program.

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

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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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