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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Remote Assessments and Genetic Determinants of 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 dystrophy type 1, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular diseaseRecruitingNot stated2026-04-01NCT07505342

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Research sitesCityCountryLinked trials
University of RochesterRochesterUnited States360