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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
InsightRP2 RegistryCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosa, retinitis pigmentosa 2RecruitingNot stated2025-05-21NCT06982417