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临床试验/JPRN-jRCT2080225082
JPRN-jRCT2080225082已完成3 期

A phase III, randomized, double masked, placebo controlled, parallel, multicenter study: To evaluate efficacy and safety of 3 % DE-089C ophthalmic solution in subject with Dry eye.

Santen pharmaceutical co.,ltd0 个研究点目标入组 300 人开始时间: 2020年2月20日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
300

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
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • •Outpatients
  • •- Both eyes diagnosed as having dry eye

排除标准

  • •- Ocular condition which affects ocular surface expect dry eye
  • •- Ocular disease which needs treatment expect dry eye
  • •- Eyelid closure failure (e.g. blepharospasm, lagophthalmos)
  • •- Anyone otherwise considered unsuitable for the study by the investigators

研究者

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