Home
Conditions
Muscular Disorders, Atrophic

Clinical trial condition

Muscular Disorders, Atrophic

Explore clinical trials studying Muscular Disorders, Atrophic. Study availability and eligibility vary by location and protocol.

621 public trials 123 recruiting studies

Refine in advanced search Browse all conditions

Muscular Disorders, Atrophic trial results

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

View Trial Details

Recruiting

Rare Glycogen Storage Diseases Natural History Study

NCT06795152

Conditions: Carbohydrate Metabolism, Inborn Errors, Cardiomyopathies, Cardiovascular Diseases, +37 more
Locations: Duke University Durham, North Carolina, United States

View Trial Details

Recruiting

A Study to Evaluate the Safety and Clinical Activity of Intramuscular Doses of BB-301 Administered to Subjects With Oculopharyngeal Muscular Dystrophy With Dysphagia

NCT06185673

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscular Diseases, +7 more
Locations: NYU Langone Health New York, United States

View Trial Details

Recruiting

Active NBS Study: Decentralised Monitoring Motor Development in Children With Duchenne Muscular Dystrophy or Spinal Muscular Atrophy Identified by Newborn Screening

NCT07286565

Conditions: Central Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), +14 more
Locations: Centre de référence des maladies neuromusculaire, Centre Hospitalier Régional de la Citadelle Liège, Belgium

View Trial Details

Recruiting

Open-label Study of WVE-N531 in Patients With Duchenne Muscular Dystrophy (FORWARD-53)

NCT04906460

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations: Arkansas Children's Hospital Little Rock, Arkansas, United States

Rare Disease Research LLC Atlanta, Georgia, United States

Istiklal Hospital/ Clinical Research Unit Amman, Jordan

The Specialty Hospital (TSH)/ Advanced Clinical Center Amman, Jordan

View Trial Details

Recruiting

Safety and Preliminary Efficacy of ULSC in Facioscapulohumeral Muscular Dystrophy (FSHD)

NCT07086521

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, FSHD - Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, +7 more
Locations: Stanford Neuroscience Health Center Palo Alto, California, United States

View Trial Details

Recruiting

The Effect of a Muscle-mimicking, Fabric-type Shoulder Orthosis on Functional Movements of the Upper Limb in Patients With Neuromuscular Disorder

NCT06363357

Conditions: ALS (Amyotrophic Lateral Sclerosis), Amyotrophic Lateral Sclerosis, Central Nervous System Diseases, +29 more
Locations: Seoul National University Hospital Seoul, Jongno-gu, South Korea

View Trial Details

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

View Trial Details

Recruiting

Extracellular RNA Biomarkers of Myotonic Dystrophy

NCT05020002

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
Locations: Massachusetts General Hospital Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center Boston, Massachusetts, United States

University of Texas Southwestern Dallas, Texas, United States

View Trial Details

Recruiting

Extracellular RNA Biomarkers of Duchenne Muscular Dystrophy

NCT05016908

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations: Boston Children's Hospital Boston, Massachusetts, United States

Massachusetts General Hospital Boston, Massachusetts, United States

View Trial Details

Muscular Disorders, Atrophic

Muscular Disorders, Atrophic trial results

Related conditions