NCT02555761已完成不适用
Evaluation of the Safety and Effectiveness of Lastacaft® Ophthalmic Solution 0.25% (Alcaftadine) for the Prevention of Itching Associated With Allergic Conjunctivitis: A Postmarketing Surveillance Study in Korea
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
- Allergan
- 入组人数
- 3,423
- 试验地点
- 76
- 主要终点
- Number of Participants with Adverse Events
研究概览
简要总结
This post-marketing surveillance study will assess the safety and efficacy of Lastacaft® Opthalmic Solution 0.25% (Alcaftadine) for the prevention of itching associated with Allergic Conjunctivitis as prescribed as standard of care in clinical practice in Korea.
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
- 2 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with itching associated with allergic conjunctivitis.
排除标准
- •Patients with hypersensitivity to Lastacaft® or its components.
研究组 & 干预措施
Lastacaft®
One drop of Lastacaft® Ophthalmic Solution 0.25% (Alcaftadine) in each eye daily as prescribed as standard of care in clinical practice.
干预措施: Alcaftadine Ophthalmic Solution 0.25% (Drug)
结局指标
主要结局
Number of Participants with Adverse Events
时间窗: 2 Weeks
次要结局
未报告次要终点
研究者
研究点 (76)
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