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临床试验/NCT01613222
NCT01613222
已完成
不适用

SpO2 System Accuracy Testing

GE Healthcare1 个研究点 分布在 1 个国家目标入组 63 人2012年6月19日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Pulse Oximetry
发起方
GE Healthcare
入组人数
63
试验地点
1
主要终点
Accuracy Root Mean Square (ARMS)
状态
已完成
最后更新
7年前

概览

简要总结

A study to test the accuracy of SpO2 sensors with various patient monitors, co-oximeters, and modules.

详细描述

The U-TruSignal with different sensors is feasible for noninvasive and continuous SpO2 monitoring and meets the specified measurement accuracy when compared to a co-oximetry gold reference.

注册库
clinicaltrials.gov
开始日期
2012年6月19日
结束日期
2013年2月15日
最后更新
7年前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

发起方
GE Healthcare
责任方
Sponsor

入排标准

入选标准

  • Ability to provide written informed consent or have a legally authorized representative provide written informed consent
  • Subjects who are 18-55 years of age
  • Subjects must be willing and able to comply with study procedures
  • HbCO\<3% (for smokers only)

排除标准

  • Subject or a legally authorized representative is unable to provide written inform consent.
  • Subjects that are considered morbidly obese (defined as BMI \> 39.5),
  • Subjects with injuries, deformities or abnormalities that may prevent proper application of the device under test,
  • Smokers with COHb levels \>3% or subjects who have smoked within two (2) days. Subjects will be screened for COHb levels of \>3% with a Masimo Radical 7 (Rainbow).
  • Subjects with known respiratory conditions (uncontrolled asthma, head cold, flu, pneumonia / bronchitis, respiratory distress / respiratory or lung surgery, emphysema, COPD, lung disease),
  • Subjects with known heart or cardiovascular conditions,
  • Female subjects that are actively trying to get pregnant or are pregnant,
  • Subjects taking blood thinners or medications with aspirin or other antiplatelet medication in them (applies only to arterial draw study),
  • Subjects with Systolic blood pressure \>140mmHg,
  • Subjects with Diastolic blood pressure \>100mmHg,

结局指标

主要结局

Accuracy Root Mean Square (ARMS)

时间窗: 60 minutes

The Accuracy Root Mean Square (ARMS) calculation is used to measure accuracy of the test SpO2 device compared to reference SpO2 device. A scatterplot is created with the forehead sensor saturation on the y-axis and the measured blood saturation on the x-axis. The line of identity is drawn representing the ideal points, meaning that the forehead sensor saturation is always the same as the blood saturation. The dispersion of the actual data points around the line of identity can be measured using a statistical calculation called Arithmetic Root Mean Square (ARMS). The smaller ARMs the closer the data points lie around the line of identity, representing a more accurate sensor as accurate and appropriate. Data analysis follows ISO 80601-2-61, 2011, Annex EE and the FDA Guidance Document for Pulse Oximeters (FDA Draft Guidance, July 19, 2007).

研究点 (1)

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