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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Registered Observational Cohort Study of Myotonic Dystrophy Type 1Congenital, 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 diseaseEnrolling by invitationNot stated2025-05-18NCT06979024

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Research sitesCityCountryLinked trials
First Affiliated Hospital of Fujian Medical UniversityFuzhouChina5