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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Prospective Exploratory Cohort Study on Ganglion Cell Degeneration in Retinitis Pigmentosa PatientsCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosaEnrolling by invitationNot stated2025-07-09NCT07056738

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OrganizationsLinked trials
University Medical Center Goettingen28

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