Cosopt Versus Xalatan
Completed · Phase 4 · Has a placebo group
Conditions studied: Open-Angle Glaucoma, Ocular Hypertension
In brief
To compare the 24-hour efficacy and safety, measured every three hours, of the dorzolamide/timolol fixed combination given twice daily versus latanoprost and placebo each given once daily.
Key facts
- Study ID
- NCT00273429
- Run by
- Pharmaceutical Research Network
- Starts
- 2005-04-01
- Expected to finish
- 2005-12-01
- Last updated by the study team
- 2007-01-09
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- adults with primary open-angle, pigmentary, or exfoliation glaucoma, or ocular hypertenstion
- intraocular pressure should be 22 to 30 mm Hg inclusive on timolol BID at the 08:00 H
- ETDRS visual acuity must be 1.0 or better in both eyes
You may not qualify if…
- any contraindications to study medications
- any anticipated change in systemic hypertensive therapy during the trial
Where it is running
- Central Florida Eye Associates — Lakeland, Florida, United States
- Midwest Eye Center SC — Bourbonnais, Illinois, United States
Full record on ClinicalTrials.gov
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