JPRN-UMIN000009071已完成未知
Evaluation of efficacy of diquafosol sodium ophthalmic solution and sodium hyaluronate ophthalmic solution on treatment of dry eye (multicenter study). - Evaluation of efficacy of diquafosol sodium ophthalmic solution and sodium hyaluronate ophthalmic solution on treatment of dry eye (multicenter study).
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 200
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
- 20years-old 至 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1) Patients who use artificial tears eyedrops within 2 weeks before a study starts. 2) Patients who need to use eyedrops other than test drugs during a study . 3) Patients who have anatomically and functionally abnormal eyelid. 4) Patients who develop allergic conjunctivitis disease requiring treatment when a study starts. 5) Patients who underwent ophthalmic surgery within 3 months before study starts ( however LASIK within 6 months). 6) Patient who have a previous history of treatment intended to become obstructed lacrimal puncta. 7) Patients who have a previous allergy to drugs that they use during a study.
研究者
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