Clinical Trials Directory

Trials / Completed

CompletedNCT01025024

Investigation of Genetic Disease Marker Associated With Korean Glaucoma Patients

Investigation of Genetic Disease Marker Associated With Korean Glaucoma Patients Patients, A Single-nucleotide Polymorphism(SNP)Analysis for Primary Open Angle Glaucoma

Status
Completed
Phase
Study type
Observational
Enrollment
1,224 (actual)
Sponsor
Chungnam National University · Academic / Other
Sex
All
Age
30 Years
Healthy volunteers
Accepted

Summary

A single-nucleotide polymorphism (SNP) analysis of DNA obtained from peripheral blood of the glaucoma patients and the normal control will be performed to find genetic marker for primary open angle glaucoma.

Detailed description

Unrelated Korean subjects who have primary open angle glaucoma were recruited in the current study. Genotyping for various SNP associated with POAG due to the linkage disequilibrium patterns is to be performed. Genotypes would be statistically compared between patients with primary open angle glaucoma and normal control subjects free of any eye diseases.

Conditions

Interventions

TypeNameDescription
GENETICSNP analysis of the DNASNP analysis of the DNA obtained from peripheral blood sample

Timeline

Start date
2007-01-01
Primary completion
2009-10-01
Completion
2009-11-01
First posted
2009-12-03
Last updated
2009-12-03

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01025024. Inclusion in this directory is not an endorsement.