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临床试验/NCT05571982
NCT05571982已完成不适用

Comparison of the Efficacy of Tidal Volume Breathing and Vital Capacity Breathing During High-flow Nasal Oxygen

Yonsei University1 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2022年10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
58
试验地点
1
主要终点
End-tidal O2

研究概览

简要总结

The purpose of this study is to compare the preoxygenation efficacy of tidal volume breathing and vital capacity breathing.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
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
否

入选标准

  • •Adult patients 20 years of age or older who are planning to undergo surgery under general anesthesia

排除标准

  • •basal skull fracture, 2번 - facial anomaly, 3번 - consciousness disorder, 4번 - Risk of aspiration

研究组 & 干预措施

Tidal volume breathing technique

Experimental

High-flow nasal oxygen will be applied to the patients through nasal openings using Optiflow system before anesthetic induction. Tidal volume breathing will be applied. Pulse oximetry, end-tidal O2, and oxygen reserve index will be monitored continuously.

干预措施: Tidal volume breathing technique (Procedure)

Vital capacity breathing technique

Active Comparator

High-flow nasal oxygen will be applied to the patients through nasal openings using Optiflow system before anesthetic induction. Vital capacity breathing will be applied. Pulse oximetry, end-tidal O2, and oxygen reserve index will be monitored continuously.

干预措施: Vital capacity breathing technique (Procedure)

结局指标

主要结局

End-tidal O2

时间窗: for 10 minutes before anesthetic induction. At Day 0.

End-tidal O2 will be monitored continuously before anesthetic induction.

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 (1)

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