Evaluation of role of oral supplementation of Vitamin B12 and folate in Open Angle Glaucoma
Not Applicable
- Conditions
- Health Condition 1: H401- Open-angle glaucoma
- Registration Number
- CTRI/2024/08/072110
- Lead Sponsor
- Post Graduate Institute of Medicine Education and Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients diagnosed with Primary open angle glaucoma, normal tension glaucoma and pseudoexfolaituve glaucoma on medical management and give their consent for enrollment in trial.
Exclusion Criteria
Patient with age less than 40 years and more than 70 years with preexisting colour vision deficiency and best corrected visual acuity of less than 20/40 due to reasons other than glaucoma.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome will be to analyze the progression of glaucoma after oral supplementation of Vitamin B 12 and folate.Timepoint: This will be done at the presentation and after 6 months of follow up.
- Secondary Outcome Measures
Name Time Method The secondary outcome will be to analyze the correlation between serum levels of Vitamin B 12 ad folate in glaucoma progression.Timepoint: This will be done at the presentation & after 6 months of follow up.