NCT00676637已完成不适用
A Pilot Study of Adherence Assessment With the Travalert™ Dosing Aid in Patients With Ocular Hypertension or Primary Open-Angle Glaucoma Who Are Treated With the Travoprost/Timolol Maleate Fixed Combination Every Evening
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
- 入组人数
- 55
- 试验地点
- 4
- 主要终点
- Mean Change from Baseline in Intraocular Pressure at 4 months
研究概览
简要总结
The purpose of this study is evaluate adherence to DuoTrav® when reinforced by the use of the Travalert™ Dosing Aid.
详细描述
This study was conducted in France, UK, Italy, and Netherlands. An identical study was conducted in Spain under Protocol ID EMD-07-02. A combined enrollment number is presented.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
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
- 未提供
排除标准
- 未提供
研究组 & 干预措施
Travalert with DuoTrav
One drop in study eye(s) once daily in the evening for four months
干预措施: Travoprost 0.004%/timolol 0.05% fixed combination eye drops (DuoTrav) (Drug)
Travalert with DuoTrav
One drop in study eye(s) once daily in the evening for four months
干预措施: Travalert Dosing Aid (Device)
结局指标
主要结局
Mean Change from Baseline in Intraocular Pressure at 4 months
时间窗: Baseline, 4 months
As measured by Goldmann applanation tonometry
次要结局
未报告次要终点
研究者
研究点 (4)
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