The Effect of Transcutaneous Electrical Nerve Stimulation on Pain During Venous Cannulation
- 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
- outpatients who underwent plastic surgery
- 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
Group Intervention Description active TENS group Transcutaneous 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 group Transcutaneous 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
Name Time Method The effect of transcutaneous electrical nerve stimulation on pain during venous cannulation 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
- Secondary Outcome Measures
Name Time Method