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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Natural History of Oculo-Pharyngeal Muscular Dystrophy (OPMD) - Israel National OPMD RegistryCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Deglutition Disorders, Digestive System Diseases, Muscle Weakness, Muscular Disorders, Atrophic, Neurologic Manifestations, Neuromuscular Manifestations, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Pharyngeal Diseases, Signs and Symptoms, digestive system disorder, esophageal disorder, eye disorder, eyelid disorder, hereditary disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, nervous system disorder, neuromuscular disease, oculopharyngeal muscular dystrophy, otorhinolaryngologic disease, ptosisRecruitingNot stated2025-08-28NCT07146256

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Research sitesCityCountryLinked trials
Sheba Medical CenterRamat GanIsrael43