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临床试验/JPRN-UMIN000040896
JPRN-UMIN000040896已完成未知

The prospective observational study for the efficacy and safety of patients using Ailamide combination ophthalmic suspension with concomitant prostaglandin analogs or prostaglandin analogs / b-blocker combination drug - Study for the efficacy and safety of patients using Ailamide with concomitant prostaglandin analogs or prostaglandin analogs / b-blocker combination drug

Department of Ophthalmology, The University of Tokyo0 个研究点目标入组 101 人开始时间: 2020年6月26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
101

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

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.Use of other IOP lowering drug or corticosteroid within past 90 days 2.History of surgical treatment for glaucoma 3.History of intraocular surgery within past 90 days 4.Treatment of a triamcinolone acetonide within past 180 days 5.Presence of any active retinal disease which may progress 6.Presence of any active ocular disease other than POAG or ocular hypertension 7.Presence of a serious systemic disease 8.Presence of corneal abnormality which is considered to preclude accurate measurement of IOP by Goldmann applanation tonometer 9.History of corneal transplantation or keratorefractive surgery 10.Decided to be inappropriate for this study by a physician in charge accurate measurement of IOP by Goldmann applanation tonometer 9.History of corneal transplantation or keratorefractive surgery 10.Decided to be inappropriate for this study by a physician in charge

研究者

发起方
Department of Ophthalmology, The University of Tokyo

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