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Study identifier: NCT02886611 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Limbus Corneae  ·  Sponsor: Fondation Ophtalmologique Adolphe de Rothschild

PhaseN/A
Planned participants60
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Amélie YAVCHITZ, MD, PhD  ·  0033148036454  ·  ayavchitz@for.paris

Always discuss trial participation with your own doctor first.

Locations (1)

Fondation Ophtalmologique Adolphe de RothschildParis, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT02886611