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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

Recruiting

Amino Acids and Exercise in FSHD

NCT07543016

Conditions: Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, FSH Muscular Dystrophy, +10 more
Locations: Criams Sport Medicine Centre Voghera, Pavia, Italy

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Recruiting

Muscle Health Measurements Using Electrical Impedance Myography

NCT07502989

Conditions: Congenital Myopathy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Distal Myopathies, +16 more
Locations: Beth Israel Deaconess Medical Center Boston, Massachusetts, United States

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Recruiting

Modifying Factors in Striated Muscle Laminopathies

NCT05394506

Conditions: Autosomal Emery-Dreifuss Muscular Dystrophy, Cardiomegaly, Cardiomyopathies, +17 more
Locations: Centre de référence maladies neuromusculaires, Hôpital Femme Mère Enfant, CHU Lyon Bron, Auvergne-Rhône-Alpes, France

Centre de référence maladies neuromusculaires, Institut de myologie, Hôpital Pitié-Salpêtrière Paris, France

Service de Neuropédiatrie, Centre de Référence Maladies Neuromusculaires, CHU de Montpellier Montpellier, Hérault, France

Service de Génétique médicale, CHU Rennes Rennes, Ille-et-Vilaine, France

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Recruiting

A Study to Evaluate the Safety of AB-1003 (Previously LION-101) in Subjects With Genetic Confirmation of LGMD2I/R9 (Part1)

NCT05230459

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, FKRP, FKRP Mutation, +17 more
Locations: University of California - Irvine Irvine, California, United States

University of Iowa Iowa City, Iowa, United States

University of Kansas Medical Center Kansas City, Kansas, United States

Kennedy Krieger Institute Baltimore, Maryland, United States

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Recruiting

Development of Quantitative Muscle Imaging as a Biomarker of Disease Endpoints in Myotonic Dystrophy

NCT07362875

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
Locations: Wake Forest University Health Sciences Winston-Salem, North Carolina, United States

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Recruiting

Observational Study to Observe Variations of Gait Parameters in Patients With Neuromuscular Diseases

NCT06666816

Conditions: Central Nervous System Diseases, Charcot Marie Tooth Disease, Charcot-Marie-Tooth Disease, +20 more
Locations: Scientific Institute IRCCS E. Medea - Sede di Bosisio Parini Bosisio Parini, Lecco, Italy

Scientific Institute IRCCS E. Medea - Polo di Conegliano Conegliano, Treviso, Italy

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Recruiting

Feasibility of the BrainGate2 Neural Interface System in Persons With Tetraplegia (BG-Speech-02)

NCT06094205

Conditions: Amyotrophic Lateral Sclerosis, Anarthria, Articulation Disorders, +44 more
Locations: University of California, Davis Sacramento, California, United States

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Recruiting

Long-Term Development of Muscular Dystrophy Outcome Assessments

NCT05989620

Conditions: Cardiomyopathies, Cardiovascular Diseases, Cobblestone Lissencephaly, +70 more
Locations: Virginia Commonwealth University Richmond, Virginia, United States

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Recruiting

Evaluating Long-term Use of a Pediatric Robotic Exoskeleton (P.REX/Agilik) to Improve Gait in Children With Movement Disorders

NCT05726591

Conditions: Brain Damage, Chronic, Brain Diseases, Central Nervous System Diseases, +16 more
Locations: National Institutes of Health Clinical Center Bethesda, Maryland, United States

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Recruiting

Myotonic Dystrophy and Facioscapulohumeral Muscular Dystrophy Registry

NCT00082108

Conditions: Congenital Myotonic Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy, +18 more
Locations: University of Rochester Medical Center, Department of Neurology Rochester, New York, United States

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