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临床试验/NCT02694900
NCT02694900已完成不适用

Comparison of Three Different Chest Compressions Methods During Pediatric Cardiopulmonary Resuscitation: A Pilot, Randomized Crossover Manikin Trial

Medical University of Warsaw2 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2016年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
52
试验地点
2
主要终点
chest compressions effectiveness

研究概览

简要总结

The objective of this pilot study was to compare the manual chest compressions (CC) versus CC feedback device TrueCPR vs mechanical CC device LifeLine ARM during simulated pediatric cardiopulmonary resuscitation

研究设计

研究类型
Interventional
分配方式
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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • give voluntary consent to participate in the study
  • maximum 1 year of work experience in medicine
  • minimum 10 clinical resuscitations
  • paramedics, nurses, physicians

排除标准

  • not meet the above criteria
  • wrist or low back diseases
  • pregnancy

结局指标

主要结局

chest compressions effectiveness

时间窗: 1 day

the percentage of correct chest compressions relative to the total number of chest compressions

次要结局

  • Depth(1 day)
  • Ease-of-use(1 day)
  • Pressure point(1 day)
  • Rate of chest compressions(1 day)
  • Complete pressure release(1 day)

研究者

发起方
Medical University of Warsaw
申办方类型
Other
责任方
Principal Investigator
主要研究者

Łukasz Szarpak

Principal Investigator

Medical University of Warsaw

研究点 (2)

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