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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
The United Kingdom Facioscapulohumeral Muscular Dystrophy Patient RegistryCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, facioscapulohumeral muscular dystrophy, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseRecruitingNot stated2026-08-20NCT04001582

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OrganizationsLinked trials
Newcastle University32

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Research sitesCityCountryLinked trials
John Walton Muscular Dystrophy Research CentreNewcastle upon TyneUnited Kingdom3