MedTrace Logo

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

NCT02886611 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2025-12-03

No results posted yet for this 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.

Conditions

  • Limbus Corneae

Sponsors & Collaborators

  • Fondation Ophtalmologique Adolphe de Rothschild

    lead NETWORK

Principal Investigators

  • Anna GEMAHLING, MD · Hôpital Fondation Adolphe de Rothschild

  • Eric GABISON, MD · Hôpital Bichat (AP-HP)

  • Dominique BREMOND-GIGNAC, MD · Hopital Necker-enfants malades (AP-HP)

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-12-15
Primary Completion
2025-12-31
Completion
2026-12-31

Countries

  • France

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02886611 on ClinicalTrials.gov