Centre de référence des maladies neuromusculaire, Centre Hospitalier Régional de la Citadelle | ClinicalTrials HQ

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Digital Monitoring of Upper Limb Function in Non-Ambulant DMD	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 applicable	2026-06-23		NCT07664124
Gait Analysis Parameter and Upper Limb Evaluation in Control Participants	Healthy Participants	Recruiting	Not applicable	2026-05-19		NCT07136506
Natural History Study for Patients With Nemaline Myopathy in Belgium	congenital structural myopathy, muscle tissue disorder, musculoskeletal system disorder, nemaline myopathy, nervous system disorder, neuromuscular disease	Not yet recruiting	Not applicable	2026-03-25		NCT07201636
Active NBS Study: Decentralised Monitoring Motor Development in Children With Duchenne Muscular Dystrophy or Spinal Muscular Atrophy Identified by Newborn Screening	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, X-linked disease, central nervous system disorder, hereditary disease, motor neuron disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, spinal cord disorder, spinal muscular atrophy	Recruiting	Not applicable	2025-12-16		NCT07286565
Gait Analysis Parameter and Upper Limb Evaluation in Adult Patients With Neurological or Metabolic Pathology	Body Weight, Charcot-Marie-Tooth disease, Cognition Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyskinesias, Huntington disease, Lambert-Eaton myasthenic syndrome, Muscular Disorders, Atrophic, Neoplasms by Site, Neurologic Manifestations, Nutritional and Metabolic Diseases, Ocular Motility Disorders, Overweight, Paraneoplastic Syndromes, Nervous System, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Spinocerebellar Ataxias, Spinocerebellar Degenerations, atactic disorder, non-human animal, autoimmune disease, autoimmune disorder of the nervous system, basal ganglia disorder, brain disorder, central nervous system disorder, central nervous system malformation, cerebellar ataxia, cerebellar disorder, choreatic disease, cognitive disorder, cranial nerve neuropathy, dementia, eye disorder, facioscapulohumeral muscular dystrophy, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, immune system disorder, inherited neurodegenerative disorder, movement disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myasthenia gravis, myotonic dystrophy, myotonic syndrome, neoplasm, nervous system disorder, neurodegenerative disease, neuromuscular disease, neuromuscular junction disease, nutritional disorder, obesity disorder, ophthalmoplegia, overnutrition, palsy, paraneoplastic syndrome, peripheral nervous system disorder, polyneuropathy, psychiatric disorder, spinal cord disorder, tauopathy	Recruiting	Not applicable	2025-08-22		NCT07136844
Holter of Movement in Patients With Amyotrophic Lateral Sclerosis.	Nutritional and Metabolic Diseases, TDP-43 proteinopathy, amyotrophic lateral sclerosis, central nervous system disorder, metabolic disease, motor neuron disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, proteostasis deficiencies, spinal cord disorder	Recruiting	Not stated	2025-05-19		NCT06228001