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临床试验/NCT00347802
NCT00347802已完成4 期

Diurnal Curves With Bimatoprost 0.03% Versus Travoprost 0.004%

Innovative Medical1 个研究点 分布在 1 个国家开始时间: 2006年7月4日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
试验地点
1

研究概览

简要总结

To compare the diurnal curves in patients using bimatoprost 0.03% versus travoprost 0.004% for the treatment of glaucoma or ocular hypertension.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Single

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

  • •· Male or female > 18 years of age
  • •Naive to treatment or washed off any ocular hypotensive agents
  • •Untreated IOP >19 mm Hg
  • •Diagnosis of open-angle glaucoma or ocular hypertension
  • •Ability to provide informed consent and likely to complete study

排除标准

  • •· Known contraindication to bimatoprost or travoprost, or any component of any study medication
  • •Uncontrolled systemic disease
  • •Active ocular disease other than glaucoma or ocular hypertension
  • •Required use of ocular medications other than the study medications during the study
  • •History of intraocular surgery within the last 3 months
  • •Prior discontinuation of any of the study medications for reasons related to efficacy or safety

研究者

申办方类型
Industry

研究点 (1)

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