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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Cerebrospinal Fluid Biomarkers 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 stated2025-11-24NCT06075693

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OrganizationsLinked trials
Massachusetts General Hospital758

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Research sitesCityCountryLinked trials
Massachusetts General HospitalBostonUnited States20