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

Recruiting now

Conditions studied: Limbus Corneae

In brief

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.

Key facts

Study ID

NCT02886611

Run by

Fondation Ophtalmologique Adolphe de Rothschild

People needed

60

Starts

2015-12-15

Expected to finish

2026-12-01

Last updated by the study team

2025-12-03

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• genetic pathology of ocular surface

You may not qualify if…

• Agonal glaucoma
• Low vision mostly related to retinal pathology
• Pregnant or breast feeding patient

Where it is running

• Fondation Ophtalmologique Adolphe de Rothschild — Paris, France (enrolling)

Full record on ClinicalTrials.gov

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