Actively Recruiting
Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation
Led by Fondation Ophtalmologique Adolphe de Rothschild · Updated on 2025-12-03
60
Participants Needed
1
Research Sites
572 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
Official Title
Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Genetic pathology of ocular surface
You will not qualify if you...
- Agonal glaucoma
- Low vision mostly related to retinal pathology
- Pregnant or breast feeding patient
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Fondation Ophtalmologique Adolphe de Rothschild
Paris, France, 75019
Actively Recruiting
Research Team
A
Amélie YAVCHITZ, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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