NCT00785252撤回不适用
Randomized Study of the EZIO Compared to Central Venous Lines Used for Emergency Vascular Access
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)1 个研究点 分布在 1 个国家开始时间: 2008年9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
- 撤回
- 试验地点
- 1
- 主要终点
- Time taken to place the device
研究概览
简要总结
Multicenter randomized study to compare powered intraosseous access to standard central line access for the administration of fluids and drugs for patients in the Emergency Dept.
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
- 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
- 否
入选标准
- •Over 18 years old Requires central access after peripheral access attempts have failed or are not otherwise feasible
排除标准
- •Fracture in target bone Not able to sign informed consent Excessive tissue or absence of adequate anatomical landmarks Known or suspected coagulopathies Pregnancy Patients in custody Patients with suspected great vessel injury Not fluid in English
研究组 & 干预措施
1
Experimental
EZIO
干预措施: Powered Intraosseous device (EZIO) (Device)
2
Experimental
Central line
干预措施: standard central line (Device)
结局指标
主要结局
Time taken to place the device
时间窗: ED visit
次要结局
- Incidence of complications(ED visit)
- Costs for each of the two methods(Ed visit)
研究者
研究点 (1)
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