NCT02700867已完成不适用
A Randomized Crossover Cadaver Trial Comparing Proximal Tibia and Proximal Humerus Infusion Rates Using the NIO Intraosseous Device During Simulated Cardiopulmonary Resuscitation Performed by Paramedics
Medical University of Warsaw2 个研究点 分布在 1 个国家目标入组 84 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
- 84
- 试验地点
- 2
- 主要终点
- Success rate
研究概览
简要总结
The investigators sought to compare the intraosseous access success rates of the proximal tibia and the proximal humerus using new Intraosseous access device "NIO" in an adult cadaver model during simulated 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
- 是
入选标准
- •give voluntary consent to participate in the study
- •paramedics
- •without previous experience in intraosseous devices
排除标准
- •not meet the above criteria
结局指标
主要结局
Success rate
时间窗: 1 day
Success rate of IO cannulation was defined as successful administration of infusion solutions via the performed IO access. Failure was defined as extravasation or unsuccessful (first) effort of IO insertion.
次要结局
- Time of IO insertion(1 day)
- Ease-of-use(1 day)
- first location(1 day)
研究者
Łukasz Szarpak
Principal Investigator
Medical University of Warsaw
研究点 (2)
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