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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Prospective Natural History Study of Retinitis PigmentosaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, blindness (disorder), cone-rod dystrophy, eye disorder, hereditary disease, inherited retinal dystrophy, nervous system disorder, retinal degeneration, retinal disorder, retinitis pigmentosa, vision disorderActive, not recruitingNot applicable2025-05-22NCT04285398

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OrganizationsLinked trials
SparingVision4

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Research sitesCityCountryLinked trials
CHNO XV-XX Paris - CIC 1423ParisFrance3
UPMC Eye CenterPittsburghUnited States6