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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Muscle MRI Outlining of Neuromuscular Diseases Using Artificial IntelligenceBecker muscular dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, Nutritional and Metabolic Diseases, X-linked disease, facioscapulohumeral muscular dystrophy, familial periodic paralysis, hereditary disease, hypokalemic periodic paralysis, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseNot yet recruitingNot stated2025-04-08NCT06917430

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