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临床试验/NCT02837536
NCT02837536已完成不适用

Horizontal vs. Vertical Positioning of the iCare Rebound Tonometer and Effects on Intraocular Pressure Readings

The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 107 人开始时间: 2016年6月23日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
107
试验地点
2
主要终点
IOP taken by iCare - horizontal

研究概览

简要总结

The goal of this study is to evaluate the agreement between intraocular pressure (IOP) measurements taken by iCare, held in both vertical and horizontal positions. In addition, iCare measurements will be compared against pneumotonometry measurements to assess for accuracy.

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

入选标准

  • 18 years of age or older
  • Must be able to understand and sign and informed consent form that has been approved by an Institutional Review Board/Ethics Committee

排除标准

  • Evidence of corneal epithelial defects or pathology affecting corneal rigidity
  • Use of topical ophthalmic medications (except for artificial tears)
  • History or corneal surgeries
  • Any condition that would prevent or inhibit intraocular pressure measurements using iCare or pneumotonometry
  • Evidence of ocular infection 30 days prior to enrollment
  • Allergy to proparacaine or latex

结局指标

主要结局

IOP taken by iCare - horizontal

时间窗: 1 Day

IOP taken by iCare - vertical

时间窗: 1 Day

IOP taken by pneumatonometer

时间窗: 1 Day

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Robert Feldman

M.D.

The University of Texas Health Science Center, Houston

研究点 (2)

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