Comparison of Brimonidine Purite, Dorzolamide, and Brinzolamide as Adjunctive Therapy to Prostaglandin Analogs
Completed · Phase 4
Conditions studied: Primary Open Angle Glaucoma, Ocular Hypertension
In brief
The purpose of this study is to compare the efficacy of brimonidine Purite, dorzolamide, and brinzolamide in reducing intraocular pressure when added to prostaglandin analog therapy (bimatoprost, latanoprost, or travoprost) in patients with glaucoma or ocular hypertension.
Key facts
- Study ID
- NCT00675207
- Run by
- Northwestern Ophthalmic Institute S.C.
- People needed
- 120
- Starts
- 2006-01-01
- Expected to finish
- 2007-07-01
- Last updated by the study team
- 2008-05-08
Who can join
Age: 41 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of primary open-angle glaucoma or ocular hypertension.
- Must be over 40 years of age.
- Intraocular pressure must be 18 mm Hg or higher after 6 weeks of treatment (run-in) with a prostaglandin analog (bimatoprost, latanoprost, or travoprost).
You may not qualify if…
- History of angle closure or narrow angle.
- Previous intraocular surgery.
- Laser trabeculoplasty within 3 months prior to screening.
- History of uveitis or intraocular inflammation.
- Use of medications other than the study medications that are known to affect IOP (e.g., beta-blockers, steroids, or angiotensin II blockers) within 3 months of study entry or during the study.
- Intolerance of or hypersensitivity to prostaglandin analogs, sulfonamides, alpha-agonists, or the preservative benzalkonium chloride.
- Women of childbearing age who are pregnant or not using contraception.
Where it is running
- Northwestern Ophthalmic Institute S.C. — Glenview, Illinois, United States
Full record on ClinicalTrials.gov
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