跳至主要内容
临床试验/NCT02708862
NCT02708862已完成不适用

Comparison of Emergency Department Preoxygenation Techniques in Healthy Volunteers

Hennepin Healthcare Research Institute0 个研究点目标入组 26 人开始时间: 2016年3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
26
主要终点
Exhaled Oxygen Concentration

研究概览

简要总结

Four methods of preoxygenation will be compared in healthy volunteers

详细描述

After informed consent, each volunteer will undergo the following techniques:

Simple mask at "flush" flow (40-60 L/min) Non-rebreather mask at 15 L/min Non-rebreather mask at 60 L/min Bag valve mask with one way exhalation valve at 15 L/min

After 3 minutes, the exhaled oxygen will be measured with an oxygen sensor

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Treatment
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

  • •Over 18 years old

排除标准

  • •Any active respiratory pathology (asthma, chronic obstructive pulmonary disease, other lung disease, smoking history more than 5 years)

研究组 & 干预措施

Preoxygenation

Experimental

All participants were enrolled in a single arm in which they underwent 4 interventions in series: 1) Simple mask at 60 L/min for 3 minutes 2) Non-rebreather at 15 L/min for 3 min 3) Non-rebreather at 60 L/min for 3 minutes 4) Bag valve mask at 15 L/min for 3 minutes

干预措施: Preoxygenation (Device)

结局指标

主要结局

Exhaled Oxygen Concentration

时间窗: Immediately after 3 minutes of oxygen supplementation

Subjects will blow into an oxygen sensor after each method (arm). The primary outcome will be a non-inferiority test between bag valve mask and non-rebreather at 60 L/min. The remaining tests will be completed for comparison, but not part of formal statistical testing.

次要结局

未报告次要终点

研究者

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

Brian Driver

Associate Research Director

Hennepin Healthcare Research Institute

相似试验