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临床试验/NCT02357511
NCT02357511已完成不适用

Validation of Pulse Waveform Analysis-based Continuous Noninvasive Blood Pressure Measurement Sensor

Tampere University Hospital1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2015年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
1
主要终点
Relationship between invasive and noninvasive blood pressure measurement

研究概览

简要总结

The study aims to define the sensitivity and specificity of a novel continuous noninvasive blood pressure monitor.

详细描述

A novel continuous noninvasive blood pressure monitor is compared to invasive arterial measurement at postoperative care unit after a planned operation. Monitor captures also saturation and ECG, which are compared to traditional monitoring.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
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
是

入选标准

  • •subjected to operative treatment with the need for invasive blood pressure measurement
  • •spontaneous ventilation
  • •able to give informed consent

排除标准

  • •denial by patient
  • •pacemaker

研究组 & 干预措施

Study goup

Experimental

Vital values are being measured for the time of two hours at postoperative setting at postanesthesia care unit. A novel method is compared to golden standard: invasive measurement. Also Saturation measurements are being compared between standard and study monitor.

干预措施: Study Monitor used (Device)

结局指标

主要结局

Relationship between invasive and noninvasive blood pressure measurement

时间窗: 2 hours of continuous measurement at PACU

comparability of study monitor systolic, diastolic and mean blood pressure to invasive blood pressure measurement

次要结局

  • Relationship between study monitor Sp02 measurement and current sp02 measurement(2 hours of continuous measurement at PACU)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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