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Prospective Natural History Study of Retinitis Pigmentosa — PHENOROD2  

Retinitis Pigmentosa Clinical Trial

Official title:
Natural History Study of Retinitis Pigmentosa Due to RHO, PDE6a or PDE6b Mutations

Clinical Trial Summary

This is natural history study of rods and cones degenerations in patients with Retinitis Pigmentosa (RP) caused by pathogenic mutations in RHO, PDE6a or PDE6b gene mutations.

Clinical Trial Description

This is an open, longitudinal, prospective, multicentric study to describe the disease progression in patients with retinitis pigmentosa due to mutation in genes with selective expression in rods: rhodopsin (RHO), phosphodiesterase 6a (PDE6a) or phosphodiesterase 6b (PDE6b).RHO,PDE6A or PDE6B mutation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04285398
Study type Interventional
Source SparingVision
Contact
Status Active, not recruiting
Phase N/A
Start date February 12, 2020
Completion date June 30, 2026
View Details
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