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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
Oral N-acetylcysteine for Retinitis PigmentosaAbnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deaf-Blind Disorders, Deafness, Ear Diseases, Eye Diseases, Hereditary, Hearing Loss, Sensorineural, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Usher syndrome, blindness (disorder), eye disorder, hearing disorder, hearing loss disorder, hereditary disease, inherited retinal dystrophy, nervous system disorder, otorhinolaryngologic disease, retinal degeneration, retinal disorder, retinitis pigmentosa, vision disorderActive, not recruitingPhase 32026-06-15NCT05537220
Study of Serine Supplementation to Protect Vision in MacTelMacular Telangiectasia Type 2 (MacTel)Not yet recruitingPhase 32026-01-15NCT07342439
Post-Approval Study of the Implantable Miniature Telescopeage-related macular degenerationEnrolling by invitationNot applicable2018-11-16NCT01757132