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RPE65-NHS

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Clinical Trial

NCT04525261 Completed
RPE65-NHS

Natural history of patients with inherited retinal diseases due to mutations in RPE65 gene

Observational
Observational

Disease

Disease type

Retinitis Pigmentosa

Orphan drug recognition

NA

Patient type

Adult

Children

Inclusion / Exclusion

Opening date

01/05/2020

Inclusion criteria :

More

Exclusion criteria :

More

Funding

other

Members involved

Main investigators

Pr Francesco PARMEGGIANI

Representative

Italy

Low Vision Daily Life and Patients Groups (TWG5), Retinal Rare Eye Diseases (WG1)
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Dr Marzio CHIZZOLINI

Substitute

Italy

Retinal Rare Eye Diseases (WG1)
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Others investigators

Dr Giancarlo Iarossi

Substitute

Italy

Retinal Rare Eye Diseases (WG1)
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Dr Luca Buzzonetti

Representative

Italy

Anterior Segment Rare Eye Diseases (WG4)
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Dr Andrea SODI

Italy

Genetic Diagnostics (TWG6), Low Vision Daily Life and Patients Groups (TWG5), Retinal Rare Eye Diseases (WG1)
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Pr Francesco Testa

Substitute

Italy

Genetic Diagnostics (TWG6), Registries & Epidemiology (TWG7), Retinal Rare Eye Diseases (WG1)
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Pr Francesca Simonelli

Representative

Italy

Genetic Diagnostics (TWG6), National Integration (TWG9), Registries & Epidemiology (TWG7), Retinal Rare Eye Diseases (WG1)
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Dr Giacomo Maria Bacci

Substitute

Italy

Anterior Segment Rare Eye Diseases (WG4), Genetic Diagnostics (TWG6), Low Vision Daily Life and Patients Groups (TWG5), Pediatric Ophthalmology Rare Diseases (WG3), Retinal Rare Eye Diseases (WG1)
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Pr Luca Rossetti

Representative

Italy

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Pr Benedetto Falsini

Representative

Italy

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ERN EYE member investigating site

HCP : Principal 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

HCP : Others investigators