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临床试验/NCT02743299
NCT02743299已完成1 期

Investigation of a Novel Turbine-driven Ventilator for Use in Cardiopulmonary Resuscitation

University of Utah0 个研究点目标入组 24 人开始时间: 2013年4月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
24
主要终点
Respiratory rate

研究概览

简要总结

The objective of this study is to determine whether healthcare professionals trained in CPR can deliver more effective ventilations during CPR using the Handivent, a novel turbine-driven ventilator as compared to bag-valve-mask ventilations, using a manikin model. The investigators believe the Handivent will deliver a more accurate respiratory rate and tidal volume, with lower intrathoracic pressure during CPR.

详细描述

Previous studies have shown that increased respiratory rate during CPR inversely correlates with blood pressure. Higher respiratory rates increase intrathoracic pressure, which in turn decreases venous return to the heart.

In one previous study, the authors looked at 3 groups of 7 pigs, ventilated at 12 (100% O2), 30 (100%), and 30 (5% CO2, 95% 02) breaths per minute during cardiac arrest, and showed increased mortality with increasing respiratory rate. Survival rates were 6/7, 1/7, and 1/7 respectively. The results of this study led to changing the CPR guidelines in 2005 to include fewer ventilations.

The authors also observed 13 cases of CPR in the field and noted EMS personnel delivered breaths at an average of 32 bpm.

In 2012, a similar study to the current study under proposal compared a pressure-limited, pneumatically driven ventilator to bag-valve-mask in simulated CPR, using medical student volunteers. That study did not show a significant difference in tidal volumes; however, they did not record respiratory rates or mean intrathoracic pressures. Furthermore, that ventilator was pneumatically -driven and pressure limited, whereas the ventilator we propose to study is turbine-driven and can be volume/time triggered.

研究设计

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

入排标准

性别
All
接受健康志愿者
是

入选标准

  • •ACLS- certified healthcare professional

排除标准

  • 未提供

研究组 & 干预措施

CPR simulation

Experimental

CPR simulation with and without ventilator

干预措施: Handivent Ventilator (Device)

结局指标

主要结局

Respiratory rate

时间窗: RR will be the average RR during the CPR simulation, which is 8-minutes in duration.

The study will measure the respiratory rate delivered during the 8-minute CPR scenario

次要结局

  • Tidal volume(Average Vt during CPR simulation, which is 8 minutes in duration)
  • Peak Inspiratory pressure(Average PIP delivered during CPR simulation, which is 8 minutes in duration.)

研究者

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

Scott Allen

Anesthesiologist

University of Utah

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