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

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02886611

Acronym

SILOG

Enrollment

Registered

2016-09-01

Start date

2015-12-15

Completion date

2026-12-31

Last updated

2025-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Limbus Corneae

Brief 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.

Interventions

None listed

Study design

Observational model

OTHER

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

* genetic pathology of ocular surface

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
Genotype-phenotype Correlation	baseline

Countries

France

Contacts

Primary ContactAmélie YAVCHITZ, MD, PhD

ayavchitz@for.paris0033148036454

Outcome results