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临床试验/NCT05119673
NCT05119673已完成不适用

Point-of-care Ultrasound for Difficult Peripheral Vascular Access in the Emergency Department - a Randomized Controlled Trial

University of Turin, Italy1 个研究点 分布在 1 个国家目标入组 442 人开始时间: 2021年10月22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
442
试验地点
1
主要终点
number of attempts of each peripheral i.v. access placement

研究概览

简要总结

Peripheral intravenous line insertion is the most commonly performed invasive procedure in the emergency department (ED). The research hypothesis is that a biplane sonographic approach (i.e., an out-of-plane and in-plane view) might be superior to a mono-plane approach (i.e., an out-of-plane or in-plane view) obtaining a peripheral vascular access among difficult patients admitted to the ED

详细描述

Peripheral intravenous line insertion is the most commonly performed invasive procedure in the emergency department (ED). In some studies, difficult vascular access population was about 33% of evaluated patients and for most of them the "blind" method (i.e., palpation) fails in the line insertion. Ultrasound guidance often increase the success rate among these patients.

Two basic techniques were proposed for sonographic guidance, a transversal or a longitudinal approach to the chosen vessel (i.e., out-of-plane or in-plane view, respectively, "mono-plane" approach).

The availability of hand-held sonographic devices is increasing the number of emergency department were this guidance is used in a difficult vascular access population.

The Butterly iQ+ device is now able to show out-of-plane and in-plane views, simultaneously, the so called bi-plane view.

Aim of this randomized controlled trial is to test if a bi-plane sonographic vision might be able to increase the performance of trained operators in obtaining a peripheral vascular access among difficult patients admitted to the ED.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
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

  • at least one of the following criteria have to be present along with the need for a peripheral access
  • chronic renal disease/ongoing dialysis;
  • sickle cell anemia;
  • prolonged and/or frequent use of i.v. drugs;
  • difficult vascular access (after a first attempt or self-reported);
  • previously need for more than one attempts / ultrasound guidance for getting a peripheral vascular access.

排除标准

  • no consent to participate in the study.

结局指标

主要结局

number of attempts of each peripheral i.v. access placement

时间窗: Through study completion, likely of 1 year and half

The number of attempts needed for getting a peripheral i.v. access will be measured

Time needed for each peripheral i.v. access placement

时间窗: Through study completion, likely of 1 year and half

Time needed for for getting a peripheral i.v. access will be measured

次要结局

未报告次要终点

研究者

发起方
University of Turin, Italy
申办方类型
Other
责任方
Principal Investigator
主要研究者

Emanuele Pivetta

Staff physician

A.O.U. Città della Salute e della Scienza

研究点 (1)

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