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

Not Applicable
Completed
Conditions
Cannulation Pain
Interventions
Procedure: Transcutaneous electrical nerve stimulation (Empi, USA)
Registration Number
NCT01607463
Lead Sponsor
Kyungpook National University Hospital
Brief Summary

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

Detailed Description

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

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • outpatients who underwent plastic surgery
Exclusion Criteria
  • concomitant sedative or analgesic medication,
  • neurological disease.
  • all patients with potentially dangerous internal diseases (American Society of Anesthesiologists' physical status > 3).

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
active TENS groupTranscutaneous electrical nerve stimulation (Empi, USA)Two electrodes were attached to the radial side of dominant forearm. In the active TENS group, TENS was delivered via two electrodes on the venous cannulation site
Placebo groupTranscutaneous electrical nerve stimulation (Empi, USA)Two electrodes were attached to the radial side of dominant forearm. In the placebo group the TENS device had no current output although the power "on" indicator light remained active.
Primary Outcome Measures
NameTimeMethod
The effect of transcutaneous electrical nerve stimulation on pain during venous cannulationone 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

Secondary Outcome Measures
NameTimeMethod
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