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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic VariantsCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosaRecruitingNot stated2026-09-08NCT05589714
Gyrate Atrophy Ocular and Systemic StudyAtrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, eye disorder, hereditary disease, optic choroid disorder, ornithine aminotransferase deficiency, uveal disorderActive, not recruitingNot stated2026-08-17NCT05312736