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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
BetterLife FSHD: A Patient-driven Health and Research PlatformCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Muscular Disorders, Atrophic, facioscapulohumeral muscular dystrophy, facioscapulohumeral muscular dystrophy 1, facioscapulohumeral muscular dystrophy 2, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular diseaseRecruitingNot stated2026-02-20NCT07409142

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OrganizationsLinked trials
FSHD Society2

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Research sitesCityCountryLinked trials
FSHD SocietyRandolphUnited States1