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临床试验/NCT01628614
NCT01628614已完成不适用

A Study of Intraocular Pressure (IOP) Reduction in Newly Diagnosed Patients With Primary Open Angle Glaucoma (POAG) or Ocular Hypertension (OHT)

Allergan0 个研究点目标入组 4,812 人开始时间: 2010年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Allergan
入组人数
4,812
主要终点
Percentage of Patients With a Reduction in Intraocular Pressure (IOP) ≥ 5mmHg From Baseline

研究概览

简要总结

This is an observational study and will evaluate IOP reduction in newly diagnosed patients with POAG or OHT. All care (including treatment and diagnostic procedures) provided is at the discretion of the participating physicians according to their clinical judgment and the local standard of medical care.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Newly diagnosed with primary open angle glaucoma or ocular hypertension

排除标准

  • 未提供

结局指标

主要结局

Percentage of Patients With a Reduction in Intraocular Pressure (IOP) ≥ 5mmHg From Baseline

时间窗: Baseline, 14 Weeks

Percentage of patients with a reduction in IOP≥5 mmHg from baseline. IOP is a measurement of the fluid pressure inside the eye. The minimum reduction of 5 mmHg was evaluated in the eye with the highest pressure at the baseline visit.

次要结局

  • Percentage of Patients With an IOP Reduction ≥10% From Baseline(Baseline, 14 Weeks)
  • Percentage of Patients With an IOP Reduction ≥20% From Baseline(Baseline, 14 Weeks)

研究者

发起方
Allergan
申办方类型
Industry
责任方
Sponsor

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