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临床试验/JPRN-UMIN000021884
JPRN-UMIN000021884已完成未知

Clinical Research of Diquas ophthalmic solution 3% on corneal epithelial barrier function in dry eye - Clinical Research of Corneal epithelial barrier function

Collaborative joint clinical research organized with Kyorin university School of Medicine and Santen Pharmaceutical Co., Ltd.0 个研究点目标入组 20 人开始时间: 2016年4月12日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
20

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

  • Patients with a history of allergy to fluorescein Patients who have allergic conjunctivitis, and have possibilities to get worse during study phase. Experience in using Diquas ophthalmic solution 3%. The investigator or subinvestigator has judged that the patient is ineligible as study subject.

研究者

发起方
Collaborative joint clinical research organized with Kyorin university School of Medicine and Santen Pharmaceutical Co., Ltd.

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