Natural History Study in Patients With PDE6A-, PDE6B- and RHO-linked Retinitis Pigmentosa
Natural History Study in Patients With PDE6A-, PDE6B- and RHO-linked Retinitis Pigmentosa
Active, not recruiting · NCT06323772 · Registry updated 2026-05-06Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Natural History Study in Patients With PDE6A-, PDE6B- and RHO-linked Retinitis Pigmentosa | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, congenital stationary night blindness autosomal dominant 1, congenital stationary night blindness autosomal dominant 2, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosa | Active, not recruiting | Not stated | 2026-05-06 | NCT06323772 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| University Hospital Tuebingen | 123 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Institute for Ophthalmic Research, University Tübingen | Tübingen | Germany | 1 |