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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Transcutaneous 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. |
| PROCEDURE | Transcutaneous 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.