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Purpose: To compare the intraocular pressure (IOP)-lowering efficacy of topically administered bimatoprost 0.03% with la-tanoprost 0.005% in patients with ocular hypertension (OHT) or glaucoma. Design: Multicenter, investigator-masked, 6-month randomized clinical trial. Methods: After washout of glaucoma medications, patients with OHT or glaucoma were randomly as-
Purpose: To compare the intraocular pressure (IOP) -lowering efficacy of topically administered bimatoprost 0.03% with la-tanoprost 0.005% in patients with ocular hypertension (OHT) or glaucoma. Design: Multicenter, investigator-masked, 6-month randomized clinical trial . Methods: After washout of glaucoma medications, patients with OHT or glaucoma were randomly as-