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临床试验/NCT02806401
NCT02806401已完成不适用

Real-time Ultrasound-guided Axillary Venous Catheterization in Pediatric Patients: Comparison With the Landmark Technique Subclavian Vein Catheterization

Seoul National University Hospital1 个研究点 分布在 1 个国家目标入组 132 人开始时间: 2016年6月最近更新:
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
132
试验地点
1
主要终点
2nd access success rate

研究概览

简要总结

The purpose of this prospective randomized study was to compare landmark-subclavian venous access to ultrasound-guided axillary venous access when performed by pediatric anesthesiologists.

详细描述

Objective

Subclavian vein catheterization may cause various complications. The investigators will compare the real-time ultrasound-guided axillary venous access vs. the landmark method- subclavian venous access in pediatric paticipants. (the needle insertion point of ultrasound-guided axillary venous is axillary vein. and the needle insertion point of landmark method is infraclavicular subclavian vein)

Design: Prospective randomized study.

Setting: Operating room of a tertiary medical center.

Interventions: The investigators will compare the ultrasound-guided axillary vein cannulation (66 paticipants) vs. the landmark method (66 pa- ticipants).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
1 Month 至 7 Years(Child)
性别
All
接受健康志愿者

入选标准

  • surgery under general anesthesia require central venous catheterization

排除标准

  • hematoma in central vein central vein anomaly catheterization site infection

研究组 & 干预措施

landmark

Experimental

landmark method_subclavian venous cannulation

干预措施: landmark (Device)

US_Ax

Active Comparator

ultrasound guided axillary venous cannulation

干预措施: US_Ax (Device)

结局指标

主要结局

2nd access success rate

时间窗: interval between skin penetration and removal of the needle or catheter after central line insertion, an expected average of 120 seconds

次要结局

  • 1st access success rate(interval between skin penetration and removal of the needle or catheter after central line insertion, an expected average of 120 seconds)
  • 3rd access success rate(interval between skin penetration and removal of the needle or catheter after central line insertion, an expected average of 120 seconds)
  • total time(interval between skin penetration and removal of the needle or catheter after central line insertion, an expected average of 120 seconds)

研究者

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

Jin-Tae Kim

professor

Seoul National University Hospital

研究点 (1)

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