Clinical Trials Directory

Trials / Completed

CompletedNCT01607463

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Kyungpook National University Hospital · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

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

Conditions

Interventions

TypeNameDescription
PROCEDURETranscutaneous electrical nerve stimulation (Empi, USA)In the active TENS group, TENS at 80 pulsed currents per second (PPS) with a pulse duration of 200 μs were delivered for 20 minutes. Current amplitude was slowly increased until a level was reached that participants reported was the maximum level they could tolerate below pain threshold without noticeable muscle contraction and maintained this intensity.
PROCEDURETranscutaneous electrical nerve stimulation (Empi, USA)In the placebo group the TENS device had no current output although the power "on" indicator light remained active.

Timeline

Start date
2012-05-01
Primary completion
2012-05-01
Completion
2012-05-01
First posted
2012-05-30
Last updated
2012-05-30

Source: ClinicalTrials.gov record NCT01607463. Inclusion in this directory is not an endorsement.