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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Investigating Exercise in Myotonic Dystrophy Type 2 (DM2)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, Myotonic Dystrophy 2, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular diseaseRecruitingNot applicable2026-10-08NCT06716931