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

> **NCT02886611** · — · RECRUITING · sponsor: **Fondation Ophtalmologique Adolphe de Rothschild** · enrollment: 60 (estimated)

## Conditions studied

- Limbus Corneae

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT02886611
- **Lead sponsor:** Fondation Ophtalmologique Adolphe de Rothschild
- **Sponsor class:** NETWORK
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2015-12-15
- **Primary completion:** 2025-12
- **Final completion:** 2026-12
- **Target enrollment:** 60 (ESTIMATED)
- **Last updated:** 2025-12-03


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02886611

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02886611, "Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT02886611. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*