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Clinical trial

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

NCT02886611 is registered in ClinicalTrials.gov with Fondation Ophtalmologique Adolphe de Rothschild as lead sponsor.

NCT NCT02886611
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Registry record

As filed in ClinicalTrials.gov.

Title
Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation
Lead sponsor
Fondation Ophtalmologique Adolphe de Rothschild
Phase
Observational
Overall status
Recruiting
Start date
December 15, 2015
Completion date
December 31, 2026
Enrollment
60 (estimated)
Sites
1

Conditions

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

limbus corneae