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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Nomad P-KAFO StudyCNS demyelinating autoimmune disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Infections, Muscular Disorders, Atrophic, Neuroinflammatory Diseases, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Picornaviridae infectious disease, RNA Virus Infections, Signs and Symptoms, autoimmune disease, autoimmune disorder of the nervous system, brain disorder, cardiovascular disorder, central nervous system disorder, central nervous system infectious disorder, cerebrovascular disorder, demyelinating disease, enterovirus infectious disease, hereditary disease, immune system disorder, injury, multiple sclerosis, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myelitis, nervous system disorder, nervous system injury, neurodegenerative disease, neuromuscular disease, palsy, poliomyelitis, postpoliomyelitis syndrome, spinal cord disorder, spinal cord injury, stroke disorder, vascular disorder, viral infectious diseaseRecruitingNot applicable2026-05-11NCT05644522
Effects of Whole-body Electrical Muscle Stimulation Exercise on Adults With Neuromuscular DiseaseBrain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Charcot-Marie-Tooth disease, Chronic Disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Infections, Lambert-Eaton myasthenic syndrome, Lysosomal Storage Diseases, Nervous System, Muscular Disorders, Atrophic, Neoplasms by Site, Neuroinflammatory Diseases, Nutritional and Metabolic Diseases, Paraneoplastic Syndromes, Nervous System, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Picornaviridae infectious disease, RNA Virus Infections, TDP-43 proteinopathy, amyotrophic lateral sclerosis, autoimmune disease, autoimmune disorder of the nervous system, autonomic nervous system disorder, brain disorder, central nervous system disorder, central nervous system infectious disorder, central nervous system malformation, centronuclear myopathy, chronic inflammatory demyelinating polyradiculoneuropathy, congenital structural myopathy, demyelinating disease, disorder of glycogen metabolism, enterovirus infectious disease, facioscapulohumeral muscular dystrophy, glycogen storage disease II, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, immune system disorder, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inborn mitochondrial metabolism disorder, inborn mitochondrial myopathy, inclusion body myositis, inherited neurodegenerative disorder, lateral sclerosis, lysosomal storage disease, metabolic disease, motor neuron disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myasthenia gravis, myelitis, myositis disease, nemaline myopathy, neoplasm, nervous system disorder, neurodegenerative disease, neuromuscular disease, neuromuscular junction disease, orthostatic intolerance, paraneoplastic syndrome, peripheral nervous system disorder, poliomyelitis, polyneuropathy, polyradiculoneuropathy, postpoliomyelitis syndrome, primary dysautonomia, progressive muscular atrophy, proteostasis deficiencies, spinal cord disorder, spinal muscular atrophy, viral infectious diseaseRecruitingNot applicable2026-03-17NCT07478172
Comparing Functional Outcomes in Individuals Using Micro-processor Controlled Orthosis Versus Stance Control OrthosisInfections, Muscular Disorders, Atrophic, Neuroinflammatory Diseases, Picornaviridae infectious disease, RNA Virus Infections, arthritic joint disease, arthropathy, central nervous system disorder, central nervous system infectious disorder, enterovirus infectious disease, injury, muscle tissue disorder, musculoskeletal system disorder, myelitis, nervous system disorder, nervous system injury, neurodegenerative disease, neuromuscular disease, poliomyelitis, postpoliomyelitis syndrome, spinal cord disorder, spinal cord injury, viral infectious diseaseActive, not recruitingNot applicable2025-05-01NCT02089880
Impairments of Neuro-muscular Communication in Motor-Neuron Disease: A Bio-Marker for Early and Personalised DiagnosisInfections, Muscular Disorders, Atrophic, Neuroinflammatory Diseases, Nutritional and Metabolic Diseases, Picornaviridae infectious disease, RNA Virus Infections, TDP-43 proteinopathy, amyotrophic lateral sclerosis, central nervous system disorder, central nervous system infectious disorder, enterovirus infectious disease, metabolic disease, motor neuron disorder, muscle tissue disorder, musculoskeletal system disorder, myelitis, nervous system disorder, neurodegenerative disease, neuromuscular disease, poliomyelitis, postpoliomyelitis syndrome, proteostasis deficiencies, spinal cord disorder, spinal muscular atrophy, viral infectious diseaseRecruitingNot stated2022-12-23NCT05663008