跳至主要内容
临床试验/NCT04412967
NCT04412967已完成不适用

A Randomized, Controlled Comparison of Nurse-led Placement of Peripheral Venous Catheters in Overweight Patients Using Standard or Dynamic Ultrasound-guided Technique

University Hospital, Linkoeping2 个研究点 分布在 1 个国家目标入组 89 人开始时间: 2017年5月1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
89
试验地点
2
主要终点
Number of cannulation attempts

研究概览

简要总结

Overweight and obesity may be associated with difficult intravenous access leading to longer procedure time and more placement attempts of peripheral venous catheters (PVC). Dynamic ultrasound-guided short-axis needle tip navigation (DUST) may facilitate the procedure.

This was a prospective, randomized, non-blinded study to compare time and placement attempts for nurse-led standard (ST) and ultrasound guided PVC placement in 90 emergency patients with a BMI ≥25kg/m2.

Consenting patients were randomized at a 1:1 ratio to receive PVC by either ST or DUST.

Application time was defined as the time from applying stasis to visible blood in the PVC flash-chamber.

No difference in time was found (medians: ST 42 s; DUST 53.5 s, P = 0.535). There were on average 17 % less placement attempts in the DUST-group (median 1 attempt; Q1 = 1 Q3 = 1) compared to the ST-group (median 1 attempt; Q1 = 1 Q3 = 1.5), (p = 0.031). Patients reported no differences in perceived pain (p = 0.955) or perceived satisfaction (p = 0.342). Pain and subcutaneous infiltrations were the only side-effects reported (ST-group 6, DUST-group 5).

DUST does not decrease time to functional PVC but reduces the number of PVC placement attempts in patients with BMI ≥25 kg/m2.

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

  • REETS prioritization level of "Orange", "Yellow", "Green" or "Blue"
  • 18 years old
  • BMI ≥25 Kg/m2
  • Need of PVC according to Emergency department guidelines
  • Able to give written informed consent

排除标准

  • Unable or unwilling to provide informed consent
  • Life threatening patient status (REETS prioritization level of "Red")
  • Immunosuppression
  • Pregnant or lactating women
  • Blood infections
  • Puncture zone skin damaged (burns, eczema, infection)

结局指标

主要结局

Number of cannulation attempts

时间窗: 1 hour

The total number of cannulation attempts performed per patient

Time to application

时间窗: 1 hour

Application time was defined as the time from applying stasis to visible blood in the PVC flash-chamber.

次要结局

  • Perceived Pain(1 hour)
  • Patient satisfaction(1 hour)

研究者

发起方
University Hospital, Linkoeping
申办方类型
Other
责任方
Principal Investigator
主要研究者

Daniel Wilhelms

Principal Investigator

University Hospital, Linkoeping

研究点 (2)

Loading locations...

相似试验