Measurement of angle using two machines (ASOCT and UBM) in shallow angle glaucoma following peripheral iris hole.
Not Applicable
- Conditions
- Health Condition 1: H400- Glaucoma suspectHealth Condition 2: H402- Primary angle-closure glaucoma
- Registration Number
- CTRI/2021/05/033583
- Lead Sponsor
- ITIKA BERI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients of primary angle closure glaucoma
Exclusion Criteria
Any intraocular or refractive surgery, active uveitis, corneal opacity/diseases which would hinder the visualization of parameters of the eye, pregnant and lactating females.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method On UBM : <br/ ><br>Angle opening distance (AOD) at 500µm and 750µm <br/ ><br>Angle Recess area (ARA) at 500µm and 750µm <br/ ><br> <br/ ><br>Trabecular iris angle (TIA) at 500µm and 750µm <br/ ><br> <br/ ><br>On ASOCT: <br/ ><br>Angle opening distance (AOD) at 500µm and 750µm <br/ ><br>Anterior chamber angle (ACA) at 500µm and 750µm <br/ ><br>Trabecular iris space area (TISA) at 500 µm and 750 µmTimepoint: 2 weeks, 3 months and 6 months
- Secondary Outcome Measures
Name Time Method Change in central corneal thickness post Peripheral iridotomy. <br/ ><br> <br/ ><br>Change in endothelial density post peripheral iridotomyTimepoint: 2 weeks, 3 months and 6 months