跳至主要内容
临床试验/NCT03565419
NCT03565419已完成不适用

Application of Smart Glasses During Ultrasound Guided Peripheral Venous Access: a Randomized Controlled Crossover Pilot Study

Inje University2 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2018年6月20日最近更新:
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
12
试验地点
2
主要终点
time for successful blood aspiration

研究概览

简要总结

Investigators aimed to explore the feasibility of smart glasses connected to a wireless ultrasound transducer for the peripheral venous access. Residents who have basic skills of ultrasound guided procedure participate in the simulation. Each participant plays the following two roles for ultrasound guided peripheral venous access; ultrasound guided peripheral venous access with and without wearing smart glasses. The order of performing two roles is determined by a randomized process and the gap between two roles are five days. The primary outcome is the time of successful blood aspiration, and secondary outcomes are first time success rate, the number of skin puncture, the number of needle redirection, the number of head movement, and subjective difficulty.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Device Feasibility
盲法
Single (Investigator)

入排标准

性别
All
接受健康志愿者

入选标准

  • Doctors who have basic skill for the ultrasound guided procedures and agree to participate the simulation

排除标准

  • Doctors who do not agree to participate the simulation
  • Doctors who do not have basic skill for the ultrasound guided procedures

研究组 & 干预措施

Control

No Intervention

Participants conduct the ultrasound-guided peripheral cannulation while they confirm real-time images displayed on the viewer next to the phantom.

Intervention

Experimental

Participants conduct the ultrasound-guided peripheral cannulation wearing smart glasses. They confirm real-time images displayed on the viewer of smart glasses.

干预措施: Smart glasses (Device)

结局指标

主要结局

time for successful blood aspiration

时间窗: up to 1 month

duration from application of probe to successful aspiration

次要结局

  • first time success rate(up to 1 month)
  • number of skin puncture(up to 1 month)
  • number of needle redirection(up to 1 month)
  • number of head movement(up to 1 month)
  • subjective difficulty of procedure(up to 1 month)

研究者

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

Joon Min Park

Associate professor, Department of Emergency Medicine

Inje University

研究点 (2)

Loading locations...

相似试验