Swipe the table sideways for more columns.

TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Trial Readiness and Endpoint Assessment in Pediatric Myotonic Dystrophy ExtensionCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, Myotonia, Neurologic Manifestations, Neuromuscular Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, hereditary disease, inherited neurodegenerative disorder, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic dystrophy, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular diseaseRecruitingNot stated2026-08-11NCT06747884

8 results · Page 1 of 1

4 results · Page 1 of 1

Swipe the table sideways for more columns.

Research sitesCityCountryLinked trials
Arkansas Children's HospitalLittle RockUnited States82
Hospital das Clínicas, University of São Paulo School of Medicine (HCFMUSP)Cerqueira CésarBrazil1
University of Kansas Medical CenterKansas CityUnited States240
Virginia Commonwealth UniversityRichmondUnited States156