NCT01786954已完成不适用
A Comparative Study of Icare Rebound Tonometry With Other Tonometry Modalities in Patients Following Vitreoretinal Surgery.
Duke University2 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2012年10月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 68
- 试验地点
- 2
- 主要终点
- Measurement of Intraocular Pressure
研究概览
简要总结
The purpose of the study is to compare the measurement of pressure inside the eye using three different FDA-approved devices (Icare, Tonopen, and Goldmann applanation).
详细描述
The three above devices will be used to measure intraocular pressure in patients one day following vitreoretinal surgery. The underlying reason for surgery is not being considered in this study. The measured pressures will be compared across devices in eyes filled with fluid, gas, and silicone oil.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Duke Eye Center patients 18 years or older
- •capacity to give legally effective consent
- •scheduled to undergo vitreoretinal surgery
排除标准
- •individuals unable to give consent
结局指标
主要结局
Measurement of Intraocular Pressure
时间窗: postoperative day #1
The primary outcome is the measurement of intraocular pressure on postoperative day #1 following vitreoretinal surgery.
次要结局
- Adverse Events(postoperative day #1)
研究者
研究点 (2)
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