NCT00950690已完成不适用
Observational Study Assessing The Efficacy And Tolerability Of Xalatan™ In Patients With Open Angle Glaucoma And /Or Ocular Hypertension.
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.1 个研究点 分布在 1 个国家目标入组 1,289 人开始时间: 2005年7月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 1,289
- 试验地点
- 1
- 主要终点
- Intraocular Pressure
研究概览
简要总结
Efficacy data was not collected or analyzed. This study did assess safety and tolerability of Xalatan.
详细描述
- Efficacy data not collected or analyzed
- Safety and tolerability of Xalatan assessed NA
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient with ocular hypertension at least 22mg Hg
- •Patient must be over 18 years old
排除标准
- •None listed in the protocol
研究组 & 干预措施
Study Drug - Xalatan 0.005% eye drops
干预措施: Xalatan 0.005% eye drops (Drug)
结局指标
主要结局
Intraocular Pressure
时间窗: Screening, 10 days, 4 weeks and 12 weeks after beginning treatment
Intraocular pressure was measured at each visit
Humphrey Perimetry Visual Field
时间窗: Visits 1 and 4
Analysis of visual field deficits for abnormalities.
次要结局
未报告次要终点
研究者
研究点 (1)
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