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American Journal of Ophthalmology
Volume 135, Issue 1
, Pages 55-63
, January 2003
A six-month randomized clinical trial comparing the intraocular pressure-lowering efficacy of bimatoprost and latanoprost in patients with ocular hypertension or glaucoma
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| Supplementary data 1 |
Mean (±SEM) intraocular pressure (IOP) at all measurements over the course of the study. Top: 8AM; Middle: 12PM; Bottom: 4PM. Baseline mean IOPs were 25.0 ± .24 mm Hg for bimatoprost and 24.9 ± .23 mm Hg for latanoprost (P=.641) at 8AM, 24.0 ± .27 mm Hg for bimatoprost and 23.3 ± .27 mm Hg for latanoprost (P=.028) at 12 PM and 22.6 ± .28 mm Hg for bimatoprost and 22.5 ± .27 mm Hg for latanoprost (P=.529) at 4PM. All mean IOPs are significantly lower in the bimatoprost treatment group than in the latanoprost treatment group at all follow-up study visits for all three timepoints, despite the higher baseline IOP at 12 PM in the bimatoprost treatment group. |
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| Supplementary data 2 |
Table of All IOP Measurements: mm Hg (SEMs). |
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Please note that add-on components may require plug-in applications.
☆ This study was supported by Allergan, Inc. Paula Bernstein, Amy L. Batoosingh, and Scott M. Whitcup are employees of Allergan, Inc.InternetAdvance publication at ajo.com Oct 1, 2002.
PII: S0002-9394(02)01827-5
© 2003 Elsevier Science Inc. All rights reserved.
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American Journal of Ophthalmology
Volume 135, Issue 1
, Pages 55-63
, January 2003
