Crossover comparative study of latanoprost/timolol fixed combination with combined therapy comprised of latanoprost and timolol
Not Applicable
- Conditions
- glaucoma, ocular hypertension
- Registration Number
- JPRN-UMIN000005426
- Lead Sponsor
- Department of Ophthalmology, Gifu University Graduate School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
Contraindication for latanoprost or timolol MD worse than or equal to -25dB (HFA 30-2) BCVA less than 0.5 Refractive error greater than or equal to +9.0D, or less than -9.0D Goldmann applanation tomometry or disc evaluation difficult or impossible History of intraocular surgery or laser Other ocular diseases which may affect the results
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method IOP after 8-week treatment
- Secondary Outcome Measures
Name Time Method