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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
DMD Gene Variants and Cardiac Dysfunction in Young Males With DystrophinopathiesBecker muscular dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, X-linked disease, cardiomyopathy, cardiovascular disorder, heart disorder, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseRecruitingNot stated2026-04-07NCT07515235

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Research sitesCityCountryLinked trials
AHEPA University Hospital of ThessalonikiThessalonikiGreece2