Abstract | OBJECTIVE: DESIGN: Double-masked, 2-center, prospective, crossover comparison. PARTICIPANTS: METHODS: Subjects were randomized to brimonidine purite or dorzolamide, each given twice daily, for the first 6-week treatment period after a 6-week latanoprost run-in. Subjects began the opposite treatment for the second 6-week period after a 6-week latanoprost-only treatment between periods. Intraocular pressure (IOP) was measured at 8 am, 12 pm, 4 pm, 8 pm, 12 am, 4 am, and 8 am at each baseline and at the end of each treatment period. This study provided an 80% power that a 1.5-mmHg difference could be excluded between groups if 27 subjects completed the study. A standard deviation (SD) of 2.8 mmHg was assumed. MAIN OUTCOME MEASURES: RESULTS: CONCLUSIONS:
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Authors | Anastasios G P Konstas, Costas H Karabatsas, Nikolaos Lallos, Nikolaos Georgiadis, Aikaterini Kotsimpou, Jeanette A Stewart, William C Stewart |
Journal | Ophthalmology
(Ophthalmology)
Vol. 112
Issue 4
Pg. 603-8
(Apr 2005)
ISSN: 1549-4713 [Electronic] United States |
PMID | 15808251
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antihypertensive Agents
- Prostaglandins F, Synthetic
- Quinoxalines
- Sulfonamides
- Thiophenes
- Brimonidine Tartrate
- Latanoprost
- dorzolamide
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Topics |
- Aged
- Antihypertensive Agents
(adverse effects, therapeutic use)
- Brimonidine Tartrate
- Circadian Rhythm
- Cross-Over Studies
- Double-Blind Method
- Drug Therapy, Combination
- Female
- Glaucoma, Open-Angle
(drug therapy)
- Humans
- Intraocular Pressure
(drug effects)
- Latanoprost
- Male
- Prospective Studies
- Prostaglandins F, Synthetic
(adverse effects, therapeutic use)
- Quinoxalines
(adverse effects, therapeutic use)
- Safety
- Sulfonamides
(adverse effects, therapeutic use)
- Thiophenes
(adverse effects, therapeutic use)
- Visual Acuity
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