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Phenotypic and Genotypic Studies of Fuchs Endothelial Corneal Dystrophy

Phenotypic and Genotypic Studies of Fuchs Endothelial Corneal Dystrophy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20140911001
Enrollment
300
Registered
2014-09-11
Start date
2012-11-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fuchs endothelial corneal dystrophy Fuchs endothelial corneal dystrophy

Interventions

Fuchs endothelial corneal dystrophy patients
Other

Sponsors

Ratchadapiseksompotch Fund
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 100 Years

Inclusion criteria

Inclusion criteria: Older than 20 years old Patients who are diagnosed as Fuchs endothelial corneal dystrophy. Family members of FECD patients.

Exclusion criteria

Exclusion criteria: Patients who have history of intraocular surgery.

Design outcomes

Primary

MeasureTime frame
Clinical characteristic and prevalence of FECD in Thailand December 2014 obsevation

Secondary

MeasureTime frame
Genetic mutation of FECD December 2015 genetic study from blood sampling

Contacts

Public ContactVilavun Puangsricharern

Chulalongkorn University

vilavun@hotmail.com022564142

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026