Prevalence of Fuchs Endothelial Corneal Dystrophy in a Population of Dermatology Patients.

NCT ID: NCT07117071

Last Updated: 2025-08-12

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

1200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-01-02

Study Completion Date

2024-12-31

Brief Summary

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The prevalence of Fuchs Endothelial Corneal Dystrophy (FECD) varies from 3.7 to 21.6% of adults depending on the population studied (country and age class), the method of diagnosis and the definition adopted. In the absence of available data for France, we analyzed the prevalence of Fuchs Endothelial Corneal Dystrophy (FECD) in a specific sub-population.

Detailed Description

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The Primary purpose is to Estimate the prevalence of Fuchs' endothelial dystrophy in the French population in dermatology population.

Conditions

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Fuchs Endothelial Corneal Dystrophy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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screening of Fuchs endothelial corneal dystrophy

Patients with screening of Fuchs endothelial corneal dystrophy will be included.

collection of medical data

Intervention Type OTHER

collection of medical data : Age, Sex, Previous cataract surgery, Cellularity, Dermatological pathology, results of screening of Fuchs endothelial corneal dystrophy by Specular microscopy

Interventions

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collection of medical data

collection of medical data : Age, Sex, Previous cataract surgery, Cellularity, Dermatological pathology, results of screening of Fuchs endothelial corneal dystrophy by Specular microscopy

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient with screening of Fuchs endothelial corneal dystrophy

Exclusion Criteria

* Patients under guardianship
* Patients unable to receive informed consent
* Patients with anterior segment pathology (declarative) (the eye concerned will not be photographed)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de Saint Etienne

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Philippe GAIN, MD PhD

Role: PRINCIPAL_INVESTIGATOR

CHU SAINT-ETIENNE

Locations

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CHU Saint-Etienne

Saint-Etienne, , France

Site Status

Countries

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France

Other Identifiers

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IRBN1392025/CHUSTE

Identifier Type: -

Identifier Source: org_study_id

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