congenital structural myopathy
congenital structural myopathy
Explore linked clinical trials. Standard reference: MONDO:000292118 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| A Study to Check Liver Health in Boys With XLMTM, a Serious Genetic Muscle Condition | congenital structural myopathy, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neuromuscular disease | Recruiting | Not stated | 2026-09-30 | NCT06581146 | |
| Reducing Risk of Stroke and DementIa In patientS With COVert cERebrovascular Disease | central core myopathy, congenital structural myopathy, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neuromuscular disease | Not yet recruiting | Not stated | 2026-09-09 | NCT06878430 | |
| Study of ASP2957 in Male Participants With X-linked Myotubular Myopathy Who Need Ventilators | congenital structural myopathy, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neuromuscular disease | Recruiting | Phase 1 / Phase 2 | 2026-09-03 | NCT07052929 | |
| A Study of AT132 in Young Children With X-Linked Myotubular Myopathy (XLMTM) | congenital structural myopathy, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neuromuscular disease | Active, not recruiting | Phase 2 / Phase 3 | 2026-09-03 | NCT03199469 | |
| WiTNNess - TNNT1 Myopathy Natural History Study | congenital structural myopathy, hereditary skeletal muscle disorder, muscle tissue disorder, musculoskeletal system disorder, nemaline myopathy, nemaline myopathy 5, nervous system disorder, neuromuscular disease | Recruiting | Not stated | 2026-06-23 | NCT06374719 | |
| Natural History Study for Patients With Nemaline Myopathy in the UK | congenital structural myopathy, muscle tissue disorder, musculoskeletal system disorder, nemaline myopathy, nervous system disorder, neuromuscular disease | Active, not recruiting | Not stated | 2026-04-13 | NCT06670378 | |
| 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 | |
| Molecular and Genetic Studies of Congenital Myopathies | Congenital Fiber Type Disproportion, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Minicore Myopathy with External Ophthalmoplegia, Thomsen and Becker disease, central core myopathy, centronuclear myopathy, congenital structural myopathy, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, musculoskeletal system disorder, myotonic syndrome, nemaline myopathy, nervous system disorder, neurodegenerative disease, neuromuscular disease | Recruiting | Not stated | 2026-03-25 | NCT00272883 | |
| Natural History Study for Patients With Nemaline Myopathy in Spain | congenital structural myopathy, muscle tissue disorder, musculoskeletal system disorder, nemaline myopathy, nervous system disorder, neuromuscular disease | Recruiting | Not stated | 2026-03-23 | NCT07488806 | |
| Effects of Whole-body Electrical Muscle Stimulation Exercise on Adults With Neuromuscular Disease | Brain 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 disease | Recruiting | Not applicable | 2026-03-17 | NCT07478172 | |
| Smoking Cessation Intervention for Young Adults Using MTM: A Randomized Controlled Trial | Chemically-Induced Disorders, congenital structural myopathy, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neuromuscular disease, nicotine dependence, psychiatric disorder, substance-related disorder | Not yet recruiting | Not applicable | 2025-08-11 | NCT07104006 | |
| Multispectral Optoacoustic Tomography for Advanced Imaging of Centronuclear Myopathy | centronuclear myopathy, congenital structural myopathy, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neuromuscular disease | Recruiting | Not stated | 2025-06-15 | NCT07021820 | |
| Assessments in Patients With Muscular Pathology and in Control Subjects : The ActiLiège Next Study | Charcot-Marie-Tooth disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Muscular Disorders, Atrophic, X-linked disease, central nervous system malformation, centronuclear myopathy, congenital muscular dystrophy, congenital structural myopathy, facioscapulohumeral muscular dystrophy, hereditary disease, hereditary motor and sensory neuropathy, inherited neurodegenerative 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 | Recruiting | Not applicable | 2025-05-20 | NCT05982119 | |
| Myotubular and Centronuclear Myopathy Patient Registry | Myotubular Myopathy, X-Linked, centronuclear myopathy, congenital structural myopathy, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neuromuscular disease | Recruiting | Not stated | 2025-04-09 | NCT04064307 | |
| The Prevalence of RYR1-related Disease | Body Temperature Changes, Congenital Fiber Type Disproportion, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hyperthermia, Intraoperative Complications, Minicore Myopathy with External Ophthalmoplegia, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Postoperative Complications, Signs and Symptoms, Thomsen and Becker disease, central core myopathy, centronuclear myopathy, congenital myopathy, congenital structural myopathy, hereditary disease, inherited neurodegenerative disorder, malignant hyperthermia of anesthesia, muscle tissue disorder, musculoskeletal system disorder, myotonic syndrome, nemaline myopathy, nervous system disorder, neurodegenerative disease, neuromuscular disease | Not yet recruiting | Not stated | 2025-01-24 | NCT06791369 | |
| Nemaline Myopathy Clinical Research Network (NM-CTRN) | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Thomsen and Becker disease, congenital structural myopathy, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, musculoskeletal system disorder, myotonic syndrome, nemaline myopathy, nervous system disorder, neurodegenerative disease, neuromuscular disease | Not yet recruiting | Not stated | 2025-01-14 | NCT06774703 | |
| A Clinical Trial Evaluating the Safety and Efficacy of a New Light Combination Therapy Addressing Intermediate AMD | Body Temperature Changes, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Heat Stress Disorders, Hyperthermia, Lysosomal Storage Diseases, Nervous System, Nutritional and Metabolic Diseases, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, brain disorder, central core myopathy, central nervous system disorder, congenital structural myopathy, disorder of glycogen metabolism, glycogen storage disease II, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, injury, lysosomal storage disease, metabolic disease, muscle tissue disorder, musculoskeletal system disorder, nervous system disorder, neuromuscular disease | Recruiting | Not applicable | 2024-11-15 | NCT06557369 | |
| The Natural History and Muscle Fatigability of Patients With Congenital Myopathies. | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Minicore Myopathy with External Ophthalmoplegia, Thomsen and Becker disease, central core myopathy, centronuclear myopathy, congenital structural myopathy, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, musculoskeletal system disorder, myotonic syndrome, nemaline myopathy, nervous system disorder, neurodegenerative disease, neuromuscular disease | Recruiting | Not stated | 2024-08-19 | NCT06157268 |