跳至主要内容
临床试验/NCT01680666
NCT01680666已完成不适用

A Prospective Randomized Trial of Ultrasound Versus Landmark Guided Central Venous Access in Children

Stanford University3 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2009年5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
150
试验地点
3
主要终点
Success of Central Venous Cannulation at First Attempt

研究概览

简要总结

The investigators hypothesized that, in children undergoing venous cannulation for central line placement by pediatric surgeons, ultrasound-guided cannulation leads to an increase in successful venous cannulation at first attempt compared to landmark guided cannulation.

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
— 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • All patients between the ages of 0 and 18 years undergoing tunneled central venous line placement under general anesthesia

排除标准

  • Preoperative proof of non-patency of central veins
  • coagulopathy
  • access site surgeon

研究组 & 干预措施

landmark guided

Active Comparator

central line placement

干预措施: central line placement (Procedure)

ultrasound guided

Active Comparator

central line placement

干预措施: central line placement (Procedure)

ultrasound guided

Active Comparator

central line placement

干预措施: Ultrasound (Device)

结局指标

主要结局

Success of Central Venous Cannulation at First Attempt

时间窗: Up to 410 seconds

The count (%) of patients with successful central venous cannulation at first attempt is reported.

次要结局

  • Patients With Arterial Punctures(Up to 410 seconds)
  • Patients With Complications(Up to 410 seconds)
  • Success of Central Venous Cannulation Within First Three Attempts(Up to 410 seconds)
  • Time to Successful Cannulation(Up to 410 seconds)

研究者

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

Matias Bruzoni

Principle Investigator

Stanford University

研究点 (3)

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