Efficacy of TEAS On Prevention of Propofol Injection Pain in Children

  • STATUS
    Recruiting
  • days left to enroll
    43
  • participants needed
    60
  • sponsor
    Konya Meram State Hospital
Updated on 12 May 2022
Accepts healthy volunteers

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.

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.

Details
Condition Injection Site
Treatment TEAS
Clinical Study IdentifierNCT05296187
SponsorKonya Meram State Hospital
Last Modified on12 May 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

ASA I-II and aged 6-13 years patents who will undergo elective surgery under general anesthesia

Exclusion Criteria

patients with propofol allergy
patients who have renal, hepatic, cardiac, neurological, psychiatric disease
Cardiac and cranial surgery
Pacemaker
Emergency surgery and patients requiring rapid serial induction
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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