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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Imaging and Gait Analysis in FSHD PatientsCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, facioscapulohumeral muscular dystrophy, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseEnrolling by invitationNot stated2025-09-10NCT07164937

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Research sitesCityCountryLinked trials
UOC NeurologiaRomeItaly1