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临床试验/NCT00372827
NCT00372827已完成4 期

Efficacy and Safety of Timolol Maleate 0.5% Compared to Brinzolamide 1% When Added to Travoprost 0.004% in Primary Open-angle Glaucoma or Ocular Hypertension

Alcon Research2 个研究点 分布在 1 个国家目标入组 245 人开始时间: 2004年2月最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
245
试验地点
2
主要终点
Mean diurnal intraocular pressure at month 3

研究概览

简要总结

The purpose of the study is to compare the efficacy and safety of Timolol 0.5% solution to Brinzolamide 1% each given twice daily when added to Travoprost 0.004% given each evening.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who are treated with any prostaglandin analogue monotherapy (excluding unoprostone) and who have an intraocular pressure between 19 and 32 mmHg at 08:00 hours.

排除标准

  • Under 18 years

结局指标

主要结局

Mean diurnal intraocular pressure at month 3

次要结局

  • Visual acuity, Slit lamp biomicroscopy and adverse events during 3 months.
  • Individual intraocular pressures measured at 08:00, 12:00 and 16:00 at month 3.
  • Reduction from baseline in mean diurnal intraocular pressure and individual timepoints.

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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