EUCTR2005-006005-61-SI进行中(未招募)不适用
A COMPARISON OF THE EFFICACY AND SAFETY OF THE DORZOLAMIDE/TIMOLOL FIXED COMBINATION GIVEN TWICE DAILY VERSUS THE LATANOPROST/TIMOLOL FIXED COMBINATION GIVEN ONCE EVERY MORNING FOLLOWING A RUN-IN PERIOD WITH TIMOLOL GIVEN ONCE DAILY - Cosopt versus Xalacom
Pharmaceutical Research Network, LLC0 个研究点目标入组 33 人开始时间: 2006年3月8日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 33
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •- adults with primary open-angle, pseudoexfoliation, or pigment dispersion glaucoma, or ocular hypertension
- •in both eyes
- •- at baseline the intraocular pressure should be 20 to 32 mm Hg inclusive at 08:00
- •measurement (Visit 2) after dosing with timolol the evening before
- •- the intraocular pressure should be 32 mm Hg or less at all time points in both eyes at
- •- visual acuity should be 6/60 or better in the study eye(s)
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- any anticipated change in systemic hypotensive therapy during the trial
- •- use of any corticosteroids by any route for more than two weeks during the study
- •- contraindications to study medications
研究者
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