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临床试验/NCT00108017
NCT00108017已完成3 期

Randomized, Multicenter, Dbl-Masked, Parallel Study Evaluating the 24 Hr. Diurnal Ocular Hypotensive Effect of 2% Dorzolamide Hydrochloride/0.5% Timolol Maleate Combo. Ophthalmic Sol. in Patients w/ Open Angle Glaucoma or Ocular Hypertension

Merck Sharp & Dohme LLC0 个研究点目标入组 330 人开始时间: 2005年4月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
330
主要终点
24 hour diurnal IOP reduction after 8 weeks of treatment

研究概览

简要总结

This study is comparing 2 medications for glaucoma and how effective they are at controlling glaucoma over the course of an entire day.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

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

入选标准

  • •Patients with glaucoma or ocular hypertension

排除标准

  • •Other eye conditions
  • •Poor vision
  • •Recent eye surgery
  • •Use of contact lenses
  • •Nursing or pregnant women
  • •Use of some other selected medications
  • •Drug or alcohol abuse
  • •Slow heart beat
  • •Allergy or previous reaction to study drugs

结局指标

主要结局

24 hour diurnal IOP reduction after 8 weeks of treatment

时间窗: After 8 weeks of treatment

次要结局

  • IOP reduction a) from baseline at 6 weeks; b) comparison with timolol; c) comparison day versus night(At 6 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

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