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Clinical Trial Summary

Propofol, an intravenous sedative agent, frequently produces pain during injection. This study was designed to investigate whether transcutaneous electrical nerve stimulation could reduce pain during propofol injection. in minimizing propofol injection pain.


Clinical Trial Description

Twenty min after transcutaneous electrical nerve stimulation, the electrodes were removed and propofol 0.5 mg/kg was administered at the rate of 0.5 ml/sec using syringe pump. Propofol injection pain was evaluated by a study blinded anesthesiologist using a four point scale: 0=no (negative response to questioning), 1=mild pain (pain reported only in response to questioning without any behavioral sings), 2=moderate pain (pain reported in response to questioning and accompanied by a behavioral signs or pain reported spontaneously without questioning, 3=severe pain (strong vocal response or response accompanied by facial grimacing, arm withdrawal or tears). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05046054
Study type Interventional
Source Kyungpook National University Hospital
Contact Younghoon Jeon, Dr
Phone +82534205863
Email jeon68@gmail.com
Status Recruiting
Phase N/A
Start date June 1, 2021
Completion date January 30, 2022

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