Recruiting NCT02886611
Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Limbus Corneae. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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.
Primary outcome measures
- Genotype-phenotype Correlation [Time frame: baseline]
Eligibility criteria
Inclusion criteria
- genetic pathology of ocular surface
Exclusion criteria
- Agonal glaucoma
- Low vision mostly related to retinal pathology
- Pregnant or breast feeding patient
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Other
Study locations
France · 1 center
- Fondation Ophtalmologique Adolphe de Rothschild — Paris
Identifiers
NCT: NCT02886611 · EGN_2015_36