Clinical Trials Directory

Trials / Completed

CompletedNCT05296187

Efficacy of TEAS On Prevention of Propofol Injection Pain in Children

Efficacy of Transcutaneous Electrical Acupuncture Point Stimulation (TEAS) for the Prevention of Propofol Injection Pain in Children

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Konya Meram State Hospital · Academic / Other
Sex
All
Age
6 Years – 13 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DEVICETEASTranscutaneous electrical acupuncture stimulation

Timeline

Start date
2025-02-14
Primary completion
2025-08-26
Completion
2025-08-26
First posted
2022-03-25
Last updated
2026-04-09

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05296187. Inclusion in this directory is not an endorsement.