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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Prospective Observational Study to Assess the Reliability and Validity of the MLSDTCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Geographic Atrophy, Stargardt disease, eye disorder, hereditary disease, macular degeneration, retinal degeneration, retinal disorderRecruitingNot stated2025-03-24NCT06805474