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临床试验/NCT02998294
NCT02998294已完成不适用

Respiratory Volume Measure Using ExSpiron 1Xi

Yonsei University2 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2016年4月6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
63
试验地点
2
主要终点
Respiratory volume measure using ExSpiron 1Xi

研究概览

简要总结

The purpose of this study was to determine the accuracy of one-time respiratory volume measured by RVM(Respiratory Volume Monitor) compared to the one-time respiratory volume measured by mechanical ventilation in post-operative ICU patients.

详细描述

The purpose of this study was to determine the accuracy of one-time respiratory volume measured by RVM(Respiratory Volume Monitor) compared to the one-time respiratory volume measured by mechanical ventilation in post-operative ICU patients.

In addition, the investigators investigated the decrease in respiratory volume in opioid infusion after ventilator weaning in this patient, and to measure the one-time respiratory volume change by RVM during deep breathing induction using Inspirometry exercise.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • An adult patients ( ≥ age 19)
  • patients who receive mechanical ventilation in the ICU of the Severance Hospital after surgery and plans to wean the mechanical ventilation within 3 days.

排除标准

  • severe respiratory illness patients (pneumothorax, chest tube intubation status, severe restrictive respiratory disease, unilateral lung ventilation, lung transplantation status, chronic restrictive respiratory disease, hydrothorax, diaphragmatic movement disorder)
  • If the candidate can not understand and carry out the experiment contents and process

研究组 & 干预措施

Respiratory monitoring group

Experimental

干预措施: Respiratory Volume Monitor(RVM) (Device)

Respiratory monitoring group

Experimental

干预措施: artificial respirator (Device)

结局指标

主要结局

Respiratory volume measure using ExSpiron 1Xi

时间窗: during 10-minute

During mechanical ventilator, we obtained respiratory parameter from ventilator and also we collected same parameter via RVM.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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