Emery-Dreifuss muscular dystrophy | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Observatoire Des Patients Atteints de Laminopathies et Emerinopathies (Observatory for PAtients With Laminopathies and Emerinopathies)	Autosomal Emery-Dreifuss Muscular Dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Emery-Dreifuss Muscular Dystrophy 1, Emery-Dreifuss muscular dystrophy, Muscular Disorders, Atrophic, X-linked Emery-Dreifuss muscular dystrophy, X-linked disease, hereditary disease, laminopathy, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular disease	Recruiting	Not stated	2026-09-21		NCT03058185
Modifying Factors in Striated Muscle Laminopathies	Autosomal 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 disease	Recruiting	Not applicable	2026-03-04		NCT05394506
Congenital Muscle Disease Study of Patient and Family Reported Medical Information	Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Emery-Dreifuss muscular dystrophy, Eye Diseases, Hereditary, Malformations of Cortical Development, Group II, Muscular Disorders, Atrophic, Neurobehavioral Manifestations, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Thomsen and Becker disease, Wieacker-Wolff syndrome, X-linked disease, autosomal recessive limb-girdle muscular dystrophy type 2G, autosomal recessive limb-girdle muscular dystrophy type 2M, brain disorder, central nervous system disorder, central nervous system malformation, cerebral cortical dysplasia, cobblestone lissencephaly, congenital muscular dystrophy due to integrin alpha-7 deficiency, congenital myasthenic syndrome, epilepsy, eye disorder, hereditary disease, inherited neurodegenerative disorder, intellectual disability, limb-girdle muscular dystrophy, lissencephaly spectrum disorders, muscle tissue disorder, muscular dystrophy, muscular dystrophy-dystroglycanopathy, type A, musculoskeletal system disorder, myotonic syndrome, nervous system disorder, neurodegenerative disease, neurodevelopmental disorder, neuromuscular disease, neuromuscular junction disease, psychiatric disorder	Recruiting	Not stated	2021-08-09		NCT01403402