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NCT05296187 Clinical Trial

Efficacy of TEAS On Prevention of Propofol Injection Pain in Children

Injection Site Clinical Trial

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

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05296187
Other study ID # TEAS Propofol Injection Pain
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 19, 2022
Est. completion date May 30, 2023

Study information
Verified date March 2023
Source Konya Meram State Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

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.

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.

Recruitment information / eligibility
Status Recruiting
Enrollment 60
Est. completion date May 30, 2023
Est. primary completion date April 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years to 13 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• TEAS
Transcutaneous electrical acupuncture stimulation

Locations
Country Name City State
Turkey Betul Kozanhan Konya

Sponsors (1)
Lead Sponsor Collaborator
Konya Meram State Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain with propofol injection pain will be assessed using a four point behavioral scale: 1= no pain (no reaction); 2= mild pain (grimace); 3= moderate pain (grimace+cry); 4= severe pain (cry+withdrawal) 5 minutes
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