24-Hour Intraocular Pressure (IOP) Control With Travoprost/Timolol Fixed Combination
Phase 3
Completed
- Conditions
- Primary Open Angle GlaucomaExfoliation Syndrome
- Registration Number
- NCT00331240
- Lead Sponsor
- Aristotle University Of Thessaloniki
- Brief Summary
The purpose of this study is to compare the short-term (8 week) mean 24-hour intraocular pressure control and safety of TravTim fixed combination given once in the evening with placebo once in the morning versus TravTim given once in the morning with placebo once in the evening in patients with open-angle glaucoma.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 32
Inclusion Criteria
- POAG
- Exfoliation syndrome
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Exclusion Criteria
- Advanced glaucoma
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Glaucoma Unit, A University Dept of Ophthalmology, AHEPA Hospital
🇬🇷Thessaloniki, Greece