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

Limbus Corneae Clinical Trial

— SILOG  

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02886611
• Other study ID #: EGN_2015_36
• Status: Recruiting
• Start date: December 15, 2015
• Est. completion date: June 2025

Study information

• Verified date: October 2023
• Source: Fondation Ophtalmologique Adolphe de Rothschild
• Contact: Amélie YAVCHITZ, MD, PhD
• Phone: 0033148036454
• Email: ayavchitz[@]for.paris
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: June 2025
• Est. primary completion date: June 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• genetic pathology of ocular surface

Exclusion Criteria:

• Agonal glaucoma

• Low vision mostly related to retinal pathology

• Pregnant or breast feeding patient

Related Conditions & MeSH terms

• Limbus Corneae

Locations

Country	Name	City	State
France	Fondation Ophtalmologique Adolphe de Rothschild	Paris

Sponsors (1)

Lead Sponsor	Collaborator
Fondation Ophtalmologique Adolphe de Rothschild

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Genotype-phenotype Correlation		baseline