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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.

622 public trials 123 recruiting studies

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Muscular Disorders, Atrophic trial results

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Phase 2 Study Evaluating Apitegromab for the Treatment of FSHD

NCT07435129

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, FSHD, Facioscapulohumeral Muscular Dystrophy, +8 more
Locations: Not specified

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Registry for Duchenne and Becker Muscular Dystrophy

NCT07402122

Conditions: Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), +10 more
Locations: Universitätsklinikum Essen Klinik für Kinderheilkunde I Essen, Germany

Universitätsklinik Heidelberg, Zentrum für Kinder- und Jugendmedizin Heidelberg, Germany

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Factors Influencing Physical Activity Levels in Children With Duchenne Muscular Dystrophy: An ICF-CY-Based Study

NCT07369609

Conditions: Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), +10 more
Locations: Not specified

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DMD and Gamified Physiotherapy

NCT07368400

Conditions: Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), +10 more
Locations: Not specified

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Self-Efficacy Enhancement Using a Multicomponent Support Group for Caregivers of Children With DMD/SMA

NCT07356063

Conditions: Central Nervous System Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy (DMD), +14 more
Locations: Not specified

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Calcium Channel Blocker in Myotonic Dystrophy Type 1

NCT07075965

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
Locations: Not specified

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Transition to Adulthood in People With Muscular Dystrophy

NCT07101185

Conditions: Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne / Becker Muscular Dystrophy, +11 more
Locations: Unit of Rare Disease- Rehabilitation Dept Bosisio Parini, Lecco, Italy

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Muscle MRI Outlining of Neuromuscular Diseases Using Artificial Intelligence

NCT06917430

Conditions: Becker Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, FSHD - Facioscapulohumeral Muscular Dystrophy, +16 more
Locations: Not specified

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Social Cognition in Dystrophinopathies and Neurodevelopmental Disorders

NCT06874166

Conditions: Bone Diseases, Bone Diseases, Developmental, Collagen Diseases, +17 more
Locations: Not specified

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Evaluation of Brain Dysfunction in Patients with Duchene Muscular Dystrophy

NCT06732011

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations: Not specified

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Muscular Disorders, Atrophic

Muscular Disorders, Atrophic trial results

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