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Clinical Trial

NCT05408715 Recruiting, Active
ROCKET

An International Prospective Natural History Study in Children With a Type II Collagen Disorder With Short Stature

Observational
Observational

Disease

Disease type

Other

Paediatric clinical trials

Patient type

Adult

Children

Inclusion / Exclusion

Opening date

29/06/2022

Closing date

31/12/2026

Inclusion criteria :

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Exclusion criteria :

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Funding

private

Members involved

Main investigators

Pr Dominique BREMOND-GIGNAC

Representative

France

Anterior Segment Rare Eye Diseases (WG4), CPMS & Digital Medecine (TWG10), 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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Dr Susana Noval

Representative

Spain

Low Vision Daily Life and Patients Groups (TWG5), National Integration (TWG9), Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Research (TWG8), Retinal Rare Eye Diseases (WG1)
Working Group Leader
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ERN EYE member investigating site

HCP : Principal investigators

OPHTARA – AP-HP, Hôpital Necker-Enfants Malades, Paris, France

Adress

Service d'ophtalmologieBât. Lecourbe - RC149 rue de Sèvres

75 015 Paris

France