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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
The United Kingdom National Registry for Myotonic DystrophyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular diseaseRecruitingNot stated2026-10-06NCT04003363

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OrganizationsLinked trials
Newcastle University32

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