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Clinical Study of a single ciliopathy: Alström Syndrome

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Clinical Trial

NCT02890550 Completed
Clinical Study of a single ciliopathy: Alström Syndrome

Clinical Study of a single ciliopathy: Alström Syndrome.

Phase 2
Observational

Disease

Disease type

Paediatric clinical trials

Orphan drug recognition

NA

Patient type

Adult

Children

Inclusion / Exclusion

Opening date

14/04/2014

Closing date

15/07/2018

Inclusion criteria :

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Exclusion criteria :

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Funding

national institution

Members involved

Main investigators

Pr Hélène Dollfus

Representative

France

Anterior Segment Rare Eye Diseases (WG4), CPMS & Digital Medecine (TWG10), Epag, ERN-EYE Coordinating committee, 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)
Working Group Leader
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ERN EYE member investigating site

HCP : Principal investigators

CARGO, Hôpitaux Universitaires de Strasbourg, France

Adress

Hôpital Civil -Bâtiment du Centre de Recherche en Biomédecine de Strasbourg (CRBS),1 Rue Eugène Boeckel

67000 STRASBOURG

France