跳至主要内容
临床试验/JPRN-UMIN000035240
JPRN-UMIN000035240招募中未知

Efficacy of IOP reduction and safety of Eybelis ophthalmic solution 0.002% - Efficacy of IOP reduction and safety of Eybelis ophthalmic solution 0.002%

Inouye Eye Hospital0 个研究点目标入组 100 人开始时间: 2018年12月13日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
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

  • Patients with aphakic eye or implanted IOL in the eye (history of cataract surgery), Patients with cataract surgery scheduled (within the last 6 months) Patients with some corneal abnormality or other diseases which may interfere with accurate IOP measurement using Goldmann applanation tonometer Patients with a history of corneal refractive surgery Patients with active extraocular disease, inflammation or infection in the eye(s) or eyelid(s) Patients with allergy to the ingredients used in the present study Pregnant, lactating women or women who may be pregnant, and women who wish to be pregnant or can not conduct appropriate contraception during the study period

研究者

相似试验