跳至主要内容
临床试验/EUCTR2005-006005-61-SI
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

发起方
Pharmaceutical Research Network, LLC

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