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Retinitis pigmentosa: molecular diagnosis by next generation sequencing

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Clinical Trial

RSFVEN-330/2010 Completed
Retinitis pigmentosa: molecular diagnosis by next generation sequencing

Retinitis pigmentosa: molecular diagnosis by next generation sequencing.

Phase 2
Observational

Disease

Disease type

Retinitis Pigmentosa

Orphan drug recognition

No

Patient type

Adult

Children

Inclusion / Exclusion

Opening date

18/06/2013

Closing date

19/09/2016

Funding

public

Members involved

Main investigators

Dr Marzio CHIZZOLINI

Substitute

Italy

Retinal Rare Eye Diseases (WG1)
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Pr Francesco PARMEGGIANI

Representative

Italy

Low Vision Daily Life and Patients Groups (TWG5), Retinal Rare Eye Diseases (WG1)
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ERN EYE member investigating site

HCP : Principal investigators

HCP : Others investigators

Center for Retinitis Pigmentosa of the Veneto Region – Camposampiero Hospital (Azienda ULSS 6 Euganea), Padova, Italy

Adress

Centro Specializzato per la Retinite Pigmentosa della Regione Veneto U.O.C. di Oculistica (Ospedale di Camposampiero, Area Rossa, 8° Piano)Via Pietro Cosma 1

35012 Camposampiero Padova

Italy