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Recruiting

NCT Number: NCT02886611

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

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.

Recruiting

Interested in participating?

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Key information

Conditions

Sex eligibility

All sexes

Study type

Observational

Primary location

Fondation Ophtalmologique Adolphe de Rothschild

Paris, 75019, France

Location status: Recruiting

Location contact

Eric GABISON, Pr

CONTACT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • genetic pathology of ocular surface

Exclusion criteria

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

Treatment and study plan

Primary outcomes

  1. Genotype-phenotype Correlation

    Time frame: baseline

Study contacts

Contact information is provided by the study sponsor or research team.

Amélie YAVCHITZ, MD, PhD

CONTACT

[email protected]

0033148036454

Sponsors and collaborators

Lead sponsor

Fondation Ophtalmologique Adolphe de Rothschild

Network

Registry information

Acronym: SILOG

Important dates

Study start
2015
Primary completion
2025
Study completion
2026
First posted
Sep 1, 2016
Registry last updated
Dec 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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