Ireland
--:--IST
Latest
Clinical Trials in France / NCT02886611
Recruiting Observational

Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation

NCT02886611 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2015-12-15
Last updated
2025-12-03

Condition(s) studied

Limbus Corneae

Study summary

The study aims at searching for a genotype-phenotype correlation in patients with a genetic pathology of the ocular surface, in order to identify genetic abnormalities associated with the most severe clinical situations.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * genetic pathology of ocular surface Exclusion Criteria: * Agonal glaucoma * Low vision mostly related to retinal pathology * Pregnant or breast feeding patient

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Fondation Ophtalmologique Adolphe de Rothschild Paris France Recruiting

More Fondation Ophtalmologique Adolphe de Rothschild trials in France

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT02886611 on ClinicalTrials.gov ↗ ← All trials in France