Institut de Myologie, France | 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
Multimodal Study About Absence of Dp140 in Becker Muscular Dystrophy: Brain-muscle Imaging, Cognition and Muscle Function	Becker muscular dystrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, X-linked disease, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular disease	Not yet recruiting	Not stated	2026-07-31		NCT07740057
Assessment of a Portable Digital Device for Quantified Analysis of Markerless Walking in Volunteers With Neuromuscular Diseases or Asymptomatic Volunteers	Charcot-Marie-Tooth disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, Pathologic Processes, Pathological Conditions, Signs and Symptoms, central nervous system disorder, central nervous system malformation, disease, hereditary disease, hereditary motor and sensory neuropathy, inherited neurodegenerative disorder, motor neuron disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, spinal cord disorder, spinal muscular atrophy	Recruiting	Not applicable	2026-05-19		NCT07321977
Evaluating Dyspnea in Autoimmune Myasthenia Gravis "Why am I Short of Breath?"	Dyspnea, Neoplasms by Site, Paraneoplastic Syndromes, Nervous System, Pathological Conditions, Signs and Symptoms, Respiration Disorders, Signs and Symptoms, Signs and Symptoms, Respiratory, autoimmune disease, autoimmune disorder of the nervous system, immune system disorder, myasthenia gravis, neoplasm, nervous system disorder, neurodegenerative disease, neuromuscular disease, neuromuscular junction disease, paraneoplastic syndrome, respiratory system disorder	Recruiting	Not stated	2026-05-08		NCT06866652
Natural History Study of Children With LAMA2-related Dystrophies	Muscular dystrophy congenital, merosin negative	Recruiting	Not stated	2024-12-12		NCT06354790
French Observatory for Patients with Type 3 Glycogenosis	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, disorder of glycogen metabolism, glycogen storage disease III, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, metabolic disease	Recruiting	Not stated	2024-09-27		NCT06616545