Study for intraocular pressure elevation after glaucoma surgery
Not Applicable
Recruiting
- Conditions
- Primary open angle glaucoma and exfoliative glaucoma
- Registration Number
- JPRN-UMIN000042864
- Lead Sponsor
- Faculty of Life Sciences, Kumamoto University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 172
Inclusion Criteria
Not provided
Exclusion Criteria
Exclusion criteria are cases who have difficulty obtaining consent for this study due to mental diseases, or reliable inspection data e.g. due to corneal diseases, who have a contraindication for Ripasuril and Brimonidine, and whose IOP is 20 mmHg or more at 1 day after surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evel of IOP at 1 day, 1 week, 1 month, and 3 months after surgery
- Secondary Outcome Measures
Name Time Method Visual acuity, number and thickness of corneal endothelium, visual field, gonioscopy, doing condition and safety