Lumigan Versus Cosopt
Completed · Phase 4 · Has a placebo group
Conditions studied: Open-Angle Glaucoma
In brief
To compare the intraocular pressure effect and safety of the dorzolamide/timolol fixed combination given twice daily versus bimatoprost given once every evening in patients with open-angle glaucoma in patients insufficiently controlled on latanoprost monotherapy
Key facts
- Study ID
- NCT00273455
- Run by
- Pharmaceutical Research Network
- People needed
- 34
- Starts
- 2006-01-01
- Expected to finish
- 2007-05-01
- Last updated by the study team
- 2008-11-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- adults with a diagnosis of bilateral open-angle glaucoma including: primary, pigment dispersion or exfoliation in both eyes
- on no therapy the intraocular pressure should be 22-29 mm Hg inclusive at the 8:00 AM measurement
- visual acuity should be 20/200 or better in each eye
You may not qualify if…
- historical failure to respond to topical beta-blockers in a clinically meaningful manner
- any contraindication to study medications
- any anticipated change, or modification in the 6 weeks prior to Visit 1, in systemic hypertensive therapy during the trial
Where it is running
- Taustine Eye Center — Louisville, Kentucky, United States
- Glaucoma Consultants & Center for Eye Research, PA — Mt. Pleasant, South Carolina, United States
- Houston Eye Associates — Houston, Texas, United States
Full record on ClinicalTrials.gov
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