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临床试验/NCT01607463
NCT01607463已完成不适用

The Effect of Transcutaneous Electrical Nerve Stimulation on Pain During Venous Cannulation

Kyungpook National University Hospital0 个研究点目标入组 100 人开始时间: 2012年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
主要终点
The effect of transcutaneous electrical nerve stimulation on pain during venous cannulation

研究概览

简要总结

The purpose of this study was to investigate whether transcutaneous electrical nerve stimulation (TENS) could reduce pain during cannulation of vein.

详细描述

One hundred patients were allocated randomly to two groups: In the active TENS group TENS was delivered via two electrodes on the venous cannulation site (radial side of the wrist of dominant forearm) 20 min prior to venous cannulation and control group received placebo (no current) TENS. Venous cannulation with a 22 gage cannula was performed. During venous cannulation the pain intensity (0 = no pain, 10 = worst pain imaginable) was measured. Any side effects during study periods were recorded

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

性别
All
接受健康志愿者

入选标准

  • outpatients who underwent plastic surgery

排除标准

  • concomitant sedative or analgesic medication,
  • neurological disease.
  • all patients with potentially dangerous internal diseases (American Society of Anesthesiologists' physical status > 3).

结局指标

主要结局

The effect of transcutaneous electrical nerve stimulation on pain during venous cannulation

时间窗: one minute after cannulation

One hundred patients were allocated randomly to two groups: In the active TENS group TENS was delivered via two electrodes on the venous cannulation site (radial side of the wrist of dominant forearm) 20 min prior to venous cannulation and control group received placebo (no current) TENS. Venous cannulation with a 22 gage cannula was performed. One minute after venous cannulation the pain intensity (0 = no pain, 10 = worst pain imaginable) was measured. Any side effects during study periods were recorded

次要结局

未报告次要终点

研究者

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

Younghoon Jeon

Anesthesiology and Pain Medicine

Kyungpook National University Hospital

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