NL-OMON31300已完成不适用
Adherence improvement in glaucoma patients - Adherence-Travalert
Alcon Laboratories0 个研究点目标入组 1,000 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 1,000
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Diagnosis glaucoma or ocular hypertension
- •Treatment with travoprost or travoprost/timolol
排除标准
- •High risk of side effects expected from travoprost or travoprost/timolol
- •Absolute inability to administer eye drops
- •Difficulty in reading or speaking Dutch
研究者
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