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临床试验/jRCT2031240688
jRCT2031240688招募中不适用

Observer -masked comparative study of STN1014003 ophthalmic solution and latanoprost ophthalmic solution in patients with open-angle glaucoma/ocular hypertension and open-label long-term study -Phase III-

Santen pharmaceutical co.,ltd0 个研究点目标入组 230 人开始时间: 2025年3月26日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
230
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized Controlled Trial
干预模型
Parallel Assignment
主要目的
Treatment Purpose
盲法
Single Blind

入排标准

年龄范围
18age old over 至 No limit(—)
性别
All

入选标准

  • 18 years of age or older.
  • Diagnosis of OAG or OHT in both eyes
  • Best corrected visual acuity (BCVA) in any eye is 0.20 or better in decimal visual acuity
  • Willingness and ability to give signed informed consent and follow study instructions

排除标准

  • Clinically significant ocular disease
  • History of angle closure glaucoma, or narrow angles
  • Previous glaucoma intraocular surgery
  • Clinically significant systemic disease
  • Participation in any investigational study within 30 days prior to screening
  • Women of childbearing potential who are pregnant, nursing, planning a pregnancy, or not using a medically acceptable form of birth control

结局指标

主要结局

-

Mean diurnal IOP at Week 4

次要结局

未报告次要终点

研究者

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