Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation
NCT ID: NCT02886611
Last Updated: 2025-12-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
60 participants
OBSERVATIONAL
2015-12-15
2026-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Low vision mostly related to retinal pathology
* Pregnant or breast feeding patient
ALL
No
Sponsors
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Fondation Ophtalmologique Adolphe de Rothschild
NETWORK
Responsible Party
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Principal Investigators
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Anna GEMAHLING, MD
Role: PRINCIPAL_INVESTIGATOR
Hôpital Fondation Adolphe de Rothschild
Eric GABISON, MD
Role: PRINCIPAL_INVESTIGATOR
Hôpital Bichat (AP-HP)
Dominique BREMOND-GIGNAC, MD
Role: PRINCIPAL_INVESTIGATOR
Hopital Necker-enfants malades (AP-HP)
Locations
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Fondation Ophtalmologique Adolphe de Rothschild
Paris, , France
Countries
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Central Contacts
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Facility Contacts
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Eric GABISON, Pr
Role: primary
Other Identifiers
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EGN_2015_36
Identifier Type: -
Identifier Source: org_study_id
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