JPRN-UMIN000004224
Recruiting
Phase 4
Comparison study for ocular hypotensive effect of switching from Travoprost 0.004% and Timolol maleate(Timoptol®-XE ophthalmic Solution 0.5%) ,Travoprost 0.004% and long-acting 2% Carteolol to a conbined opthalmic solution Travoprost 0.004%/Timolol 0.5% - Comparison study for ocular hypotensive effect of switching from Travoprost 0.004% and Timolol maleate,Travoprost 0.004% and long-acting 2% Carteolol to a conbined opthalmic solution Travoprost 0.004%/Timolol 0.5%
Department of Ophthalmology Yokohama City University Hospital0 sites30 target enrollmentSeptember 17, 2010
ConditionsGlaucoma
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Glaucoma
- Sponsor
- Department of Ophthalmology Yokohama City University Hospital
- Enrollment
- 30
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1Patient, who has been managed due to chronic or replace uvetis, sceritis and herpes cornea. 2\.Patient, who has been managed by traumatic diseases,ocular surgery,laser operation within 3 months. 3\.Patinet, who is not available to measure by Aplanation tonomater. 4\.Patinet, who has irritation for PG eye solution, related PG eye solution and Benzalkonium chloride(BAC). 5\.Patient, who is severe Alzheimer. 6\.Patinet, who has been managed by oral CAI or steroid eye solution. 7\.Patinet, who has been applied other IOP reductive drug.
Outcomes
Primary Outcomes
Not specified
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