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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Multi-Dimensional Model of cAre and transItion for Patients With cOmplex RAre DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Muscular Disorders, Atrophic, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, body dysmorphic disorder, hereditary disease, inborn mitochondrial metabolism disorder, metabolic disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular disease, psychiatric disorder, somatoform disorderActive, not recruitingNot stated2026-04-30NCT07558213

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Research sitesCityCountryLinked trials
Fondazione Policlinico Universitario A. Gemelli IRCCSRomaItaly26