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PHENOROD1

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Clinical Trial

NCT03975543 Unknown
PHENOROD1

Retrospective Natural History Study of Retinitis Pigmentosa.

Observational
Observational

Disease

Disease type

Paediatric clinical trials

Retinitis Pigmentosa

Orphan drug recognition

NA

Patient type

Adult

Children

Inclusion / Exclusion

Closing date

31/07/2019

Inclusion criteria :

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Exclusion criteria :

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Funding

industry

Members involved

Others investigators

Pr Isabelle Audo

Representative

France

Genetic Diagnostics (TWG6), Low Vision Daily Life and Patients Groups (TWG5), National Integration (TWG9), Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), Research (TWG8), Retinal Rare Eye Diseases (WG1)
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ERN EYE member investigating site

HCP : Principal investigators