Abstract | PURPOSE: PATIENTS AND METHODS: Sixteen consecutive patients fulfilling eligibility criteria (glaucomatous optic neuropathy associated with visual field defect in at least one eye, intraocular pressure (IOP) < or = 18 mmHg (average of the two highest readings of the round-the-clock curve, including one reading at midnight in supine position), no prior glaucoma therapy, angle wide open, visual acuity 20/40 or better) were enrolled in this prospective, randomized, placebo-controlled clinical trial with crossover design, lasting 30 days for each treatment phase plus 15-day washout in between. Main outcome was IOP (average of the two highest readings of the round-the-clock curve). RESULTS: Mean IOP was significantly reduced by brimonidine (from 17.1 +/- 0.7 mm Hg to 13.9 +/- 2.2 mmHg, p<0.001 (paired Student t-test)). At the end of the 30-day brimonidine phase, 4 of 16 subjects showed a > or = 30% IOP decrease over baseline. CONCLUSIONS:
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Authors | S A Gandolfi, L Cimino, P Mora |
Journal | European journal of ophthalmology
(Eur J Ophthalmol)
2003 Aug-Sep
Vol. 13
Issue 7
Pg. 611-5
ISSN: 1120-6721 [Print] United States |
PMID | 14552594
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Antihypertensive Agents
- Ophthalmic Solutions
- Quinoxalines
- Brimonidine Tartrate
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Topics |
- Antihypertensive Agents
(therapeutic use)
- Brimonidine Tartrate
- Cross-Over Studies
- Double-Blind Method
- Female
- Glaucoma, Open-Angle
(drug therapy)
- Humans
- Intraocular Pressure
(drug effects)
- Male
- Manometry
- Middle Aged
- Ocular Hypertension
(drug therapy)
- Ophthalmic Solutions
- Placebo Effect
- Prospective Studies
- Quinoxalines
(therapeutic use)
- Treatment Outcome
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