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Clinical Trial Summary

The purpose of this study is to determine the efficacy of transcutaneous electrical acupoint stimulation for the prevention of propofol injection pain in children.


Clinical Trial Description

Pain from the injection of propofol is a common side effect during anesthetic practice. Various methods have been used to reduce this pain. This prospective, randomized study was designed to determine the efficacy of transcutaneous electrical acupuncture point stimulation in reducing propofol injection pain in children. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05296187
Study type Interventional
Source Konya Meram State Hospital
Contact
Status Recruiting
Phase N/A
Start date April 19, 2022
Completion date May 30, 2023

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