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Clinical trial

Genetic Decryption of Leber Congenital Amaurosis (LCA) in a Large Cohort of Independent Families: Establishment of Genotype-phenotype Correlations and Updating the Clinical Definition of This Retinal Dystrophy

NCT02970266 is registered in ClinicalTrials.gov with Assistance Publique - Hôpitaux de Paris as lead sponsor.

NCT NCT02970266
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Registry record

As filed in ClinicalTrials.gov.

Title
Genetic Decryption of Leber Congenital Amaurosis (LCA) in a Large Cohort of Independent Families: Establishment of Genotype-phenotype Correlations and Updating the Clinical Definition of This Retinal Dystrophy
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Phase
Observational
Overall status
Completed
Start date
September 30, 2010
Completion date
November 30, 2016
Enrollment
659 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

leber congenital amaurosis