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临床试验/JPRN-UMIN000018510
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Evaluation of efficacy of diquafosol sodium eyedrop - Evaluation of efficacy of diquafosol sodium eyedrop

Inouye Eye Hospital0 个研究点目标入组 30 人开始时间: 2015年8月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
30

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. atients who use dry eye or MGD treatment within 2 weeks before a study starts. 2. Patient who have a previous history of treatment intended to become obstructed lacrimal puncta. 3. Patients who need to use eyedrops other than test drugs during a study. 4. Patients who have anatomically and functionally abnormal eyelid. 5. Patients with surgical history in the internal eye (including laser therapy) within 3 months prior to initiation of the clinical research. 6. Patients who have a previous allergy to drugs that they use during a study. 7. Patients who have any other reasons that causes the study doctor to deem a subject unsuitable for the study

研究者

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