Comparison of latanoprost and timolol in the treatment for exfoliation glaucoma: A randomized controlled trial.
Not Applicable
- Conditions
- Exfoliation glaucoma
- Registration Number
- JPRN-C000000425
- Lead Sponsor
- Department of Ophthalmology and Visual Science, Kumamoto University Graduate School of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
1. Severe visual field defect. 2. The treatment with latanoprost or timolol within the last 28 days. 3. Allergy to latanoprost or timolol. 4. The past histories of intraocular surgery within the last 3 months or glaucoma surgery. 5. The patients with asthma, heart failure, severe diabetes mellitus or pregnancy. 6. The patients who participated in another drug study within 30 days. 7. Judged inappropriate for this study by the physicians.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method