NCT01105910已完成4 期
Efficacy of Systane Ultra in Post Menopausal Women With Dry Eye
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 70
- 主要终点
- Reduction in corneal staining
研究概览
简要总结
To evaluate the efficacy of Systane Ultra in post menopausal women with dry eye.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Double (Participant, 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
- •Post-menopausal (menses ceased more than 12 months prior to the start of the study).
- •Diagnosed for dry eye
排除标准
- •History of Sjögren's Syndrome or evidence of chronic dry eye syndrome. Confirmed autoimmune connective tissue diseases such as rheumatoid arthritis, fibromyalgia or scleroderma.
- •Active and severe blepharitis, rosacea and associated ocular sequelae.
- •Has any significant eyelid abnormality affecting lid function.
结局指标
主要结局
Reduction in corneal staining
时间窗: 30 days
次要结局
- Patient acceptability / comfort(30 days)
研究者
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