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临床试验/NCT00417703
NCT00417703已完成不适用

A Prospective Investigation of the Intraocular Pressure Immediately Following Intravitreous Injection of Ranibizumab

Oklahoma State University Center for Health Sciences1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2007年1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
入组人数
75
试验地点
1

研究概览

简要总结

This study will quantify the intraocular pressure elevation in the immediate time period following intravitreous injection. With more widespread use of intravitreous injections in patients that may require several injections per year, it is important to document the sudden increase in intraocular pressure, including the maximum intraocular pressure and the time required for the intraocular pressure to return to baseline. This data may be useful in stimulating additional studies to evaluate the long term ocular effects of repeated intravitreous injections.

We hypothesize that the intraocular pressure increases significantly following intravitreous injection and then returns to baseline during the initial thirty minutes following ranibizumab injection.

详细描述

We will assess the trend of intraocular pressure immediately following intravitreal injection of ranibizumab 0.5 mg (0.05 mL) by taking serial intraocular pressure readings every five minutes for thirty minutes after injection. This study is a prospective descriptive data collection consisting of measuring intraocular pressure immediately following intraocular injection, and at 5, 10, 15, 20, 25, and 30 minutes following injection of ranibizumab 0.5 mg.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or Female Patients >18 years of age
  • Patients will have documented choroidal neovascular membranes on fluorescein angiogram and/or optical coherence tomography
  • Requiring treatment or maintenance therapy for choroidal neovascular membrane
  • Able and willing to provide written informed consent

排除标准

  • History of arterial occlusive disease of the eye.
  • History of advanced glaucoma.

研究者

发起方
Oklahoma State University Center for Health Sciences
申办方类型
Other

研究点 (1)

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