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临床试验/JPRN-UMIN000007026
JPRN-UMIN000007026招募中未知

Efficacy IOP lowering and safety of Travoprost Ophthalmic Solution in Normal Tension Glaucoma patients. - Efficacy IOP lowering and safety of Travoprost Ophthalmic Solution in Normal Tension Glaucoma patients.

I.CHANGE study group0 个研究点目标入组 100 人开始时间: 2012年1月6日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
100

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.Complications with chronic or recurrent uveitis, scleritis, or corneal herpes. 2.History of ocular trauma or intraocular conventional surgery or laser ocular surgery in the study eye within 3 months before baseline examinations. 3.Any abnormality preventing reliable applanation tonometer in the study eye. 4.Known medical history of allergic to PGA. 5.Patients using an IOP-lowering drug other than those to be used in the study. 6.Patients using systemic administration of an oral CAI (Diamox, etc.) 7.Patient having serious eyes complications 8.Women who are pregnant or lactating. 9.Patients who are judged to be inappropriate for participation in the study for other reason by the doctor in charge.

研究者

发起方
I.CHANGE study group

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