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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 Medical2 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
2

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

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 (2)

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