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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Modifying Factors in Striated Muscle LaminopathiesAutosomal Emery-Dreifuss Muscular Dystrophy, Cardiomegaly, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Emery-Dreifuss muscular dystrophy, Muscular Disorders, Atrophic, autosomal dominant Emery-Dreifuss muscular dystrophy, cardiomyopathy, cardiovascular disorder, congenital muscular dystrophy due to LMNA mutation, dilated cardiomyopathy, heart disorder, hereditary disease, laminopathy, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseRecruitingNot applicable2026-03-04NCT05394506

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