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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Natural History Study of Retinitis Pigmentosa Type 11Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis, retinitis pigmentosa, retinitis pigmentosa 11Active, not recruitingNot stated2025-03-21NCT04805658

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OrganizationsLinked trials
Oslo University Hospital327

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Research sitesCityCountryLinked trials
Department of Ophthalmology, Oslo University HospitalOsloNorway1