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临床试验/NCT03772574
NCT03772574已完成不适用

Preoxygenation Using THRIVE and Facemask Oxygenation in Parturients

University of British Columbia2 个研究点 分布在 1 个国家目标入组 91 人开始时间: 2018年12月1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
91
试验地点
2
主要终点
Preoxygenation Duration

研究概览

简要总结

This study aims to determine the duration for pre-oxygenation using THRIVE and facemask for parturients.

详细描述

We aim to determine the duration required for THRIVE and facemask preoxygenation in parturients for them to achieve ETO2 >90%.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Pregnant patients ≥36 weeks gestation.
  • Non-laboring patients admitted for elective Cesarean delivery under neuraxial anesthesia or induction of labor.
  • American Society of Anesthesiologists (ASA) class 2.

排除标准

  • Any medical conditions that are likely to affect gas exchange.
  • Obstructed nasal passage.
  • Unable to tolerate a tight fitting facemask.
  • Body Mass Index ≥40 kg/m
  • Patients who are in active labor (i.e. cervical dilation ≥4cm).
  • Patients who are unable to give informed consent.

结局指标

主要结局

Preoxygenation Duration

时间窗: Maximum 8 minutes

Duration to achieve EtO2 \>=90% after tidal volume breathing using THRIVE and facemask pre-oxygenation.

次要结局

  • Proportion to Reach EtO2 of 90 Percent at 7 Minutes(7 minutes of preoxygenation)
  • Proportion to Reach End Tidal Oxygen (ETO2) of 90 Percent at 3 Minutes(3 minutes of pre-oxygenation)
  • Proportion to Reach EtO2 of 90 Percent at 4 Minutes(4 minutes of preoxygenation)
  • Proportion to Reach EtO2 of 90 Percent at 5 Minutes(5 minutes of preoxygenation)
  • Proportion to Reach EtO2 of 90 Percent at 8 Minutes(8 minutes of preoxygenation)
  • Comfort Score(1 minute after data collection)
  • Proportion to Reach EtO2 of 90 Percent at 6 Minutes(6 minutes of preoxygenation)
  • Acceptability Score(1 minute after data collection)

研究者

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

Anthony Chau

Clinical Assistant Professor

University of British Columbia

研究点 (2)

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