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
| Type | Name | Description |
|---|---|---|
| GENETIC | SNP analysis of the DNA | SNP 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.