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临床试验/JPRN-UMIN000009371
JPRN-UMIN000009371已完成未知

Study on evaluation of therapeutic efficacy and search for a therapeutic biomarker in dry eye with rebamipide eye drop treatment. - Evaluation of therapeutic efficacy and therapeutic biomarker in dry eye with rebamipide eye drop treatment.

Division of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine.0 个研究点目标入组 55 人开始时间: 2012年12月1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
55

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

  • a) Patients with dry eye. 1) Patients with anterior segment disease (including blepharitis, lagophthalmos, blepharospasm, iritis and conjunctivochalasis) other than dry eye (History is excluded). 2) Patients who cannot discontinue eye drops (include all eye drops such as prescribed drug and OTC medicine) except for the study drug or the control drug from the study initiation until the end of study treatment or who expect to use those drugs. 3) Patients with punctal plug or patients whose punctal plug fell off within three months prior to the study drug initiation examination. Patients with a history ofsurgical punctual occlusion are also excluded. 4) Patients with a history of surgery of the ocular surface within 12 months, or patients with a history of intraocular surgery within three months prior to the study drug initiation examination. 5) Patients who have difficulty in sampling. 6) Patients that a study supervisor or a study partaker judged participation in this study to be inappropriate. b) Non-dry eye patients 1) Patients with anterior segment disease. 2) Patients who used eye drops or the contact lens within two weeks prior to study initiation. 3) Patients with a history of surgery of the ocular surface within 12 months or patients with a history of intraocular surgery within three months prior to the study drug initiation examination. 4) Patients who have difficulty in sampling. 5) Patients that a study supervisor or a study partaker judged participation in this study to be inappropriate.

研究者

发起方
Division of Ophthalmology, Department of Visual Sciences, Nihon University School of Medicine.

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