NCT00941096已完成4 期
Efficacy Of The Bimatoprost/Timolol Fixed Combination In Patients Treated With Bimatoprost for Primary Open Angle Glaucoma, Exfoliation Glaucoma or Ocular Hypertension.
Larissa University Hospital2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2009年7月1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
- 发起方
- 入组人数
- 30
- 试验地点
- 2
- 主要终点
- Mean diurnal intraocular pressure
研究概览
简要总结
The purpose of this study is to examine the ocular hypotensive effect of Bimatoprost and the potential additional effect of the Bimatoprost/Timolol fixed combination in eyes with ocular hypertension, primary open angle glaucoma or exfoliation glaucoma.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
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
- •Primary open angle glaucoma
- •Exfoliation glaucoma
- •Ocular hypertension
排除标准
- •Younger than 18 years old
- •Inability to understand and/or follow study requirements
- •Women of childbearing potential not using reliable birth control, pregnant or lactating women
- •History of chronic obstructive pulmonary disease, heart failure, 2nd or 3rd AV block
- •Anticipated modification of treatment for systemic hypertension during the study period
- •History of ocular herpes, corneal scarring, conventional or laser surgery or macular pathology
- •History of allergy, poor tolerability or poor response to study medication
- •Best corrected visual acuity less than 0.4
- •Significant visual field defect (MD<15.0 dB)
结局指标
主要结局
Mean diurnal intraocular pressure
时间窗: Five weeks on each medication
次要结局
未报告次要终点
研究者
研究点 (2)
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