跳至主要内容
临床试验/NCT01888094
NCT01888094已完成2 期

SUBclavian Central Venous Catheters Guidance and Examination by UltraSound : a Randomized Controlled Study Versus Landmark Method

University Hospital, Clermont-Ferrand2 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2013年6月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
300
试验地点
2
主要终点
procedure time between the beginning of procedure ( TO) and when the catheter is controlled ( T4) between strategy catheter cannulation 'standard' and a strategy called "ultrasound all

研究概览

简要总结

Prospective, randomized controlled clinical unicentric study, in ICU, Cannulation of the subclavian venous and examination guided with ultrasound

详细描述

One groupe : Ultrasound guided for cannulation and examination of absence ofcomplications One groupe : landmark method and examination with chest radiography

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

入选标准

  • adults patients
  • requiring subclavian vein cannulation
  • patient covered by french health care system

排除标准

  • patient refusal
  • requiring vein cannulation femoral or jugular
  • we see nothing with echocardiography
  • children and not adult patients

结局指标

主要结局

procedure time between the beginning of procedure ( TO) and when the catheter is controlled ( T4) between strategy catheter cannulation 'standard' and a strategy called "ultrasound all

时间窗: at day 1

次要结局

  • incidence of occurrence of complications: pneumothorax, hemothorax, bad positioning (outside of the superior vena cava or the right atrium) between the two strategies(at day 1)
  • failure of technology between the two strategies.(at day 1)
  • occurrence of central venous catheter infection.(at day 1)
  • procedure time Tn-Tn (n 0-5) between the two strategies.(at day 1)

研究者

发起方
University Hospital, Clermont-Ferrand
申办方类型
Other
责任方
Sponsor

研究点 (2)

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