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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Personalized Training for People With Rare Neuromuscular DisordersCharcot-Marie-Tooth disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, central nervous system malformation, 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, polyneuropathyRecruitingNot applicable2026-06-18NCT06708468
Norwegian Spontaneous Coronary Artery Dissection StudyInfarction, Necrosis, Pathologic Processes, Pathological Conditions, Signs and Symptoms, cardiovascular disorder, heart disorder, ischemic disease, myocardial infarction, myocardial ischemia, short chain acyl-CoA dehydrogenase deficiency, vascular disorderRecruitingNot stated2026-01-05NCT07317323