NCT03959605View on ClinicalTrials.gov

Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children

CompletedOBSERVATIONAL
Enrollment

48

Participants

Timeline

Start Date

January 6, 2019

Primary Completion Date

February 2, 2021

Study Completion Date

October 1, 2021

Conditions
Albinism, Ocular
Interventions
GENETIC

blood sample for genetic test

detection of pathogenic variants among the 19 genes known to be involved in albinism

DIAGNOSTIC_TEST

Ophtalmological examination

measurement of visual acuity, OCT and OCTA

Trial Locations (1)

75019

Fondation A de Rothschild, Paris

All Listed Sponsors
lead

Fondation Ophtalmologique Adolphe de Rothschild

NETWORK

NCT03959605 - Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children | Biotech Hunter | Biotech Hunter