CompletedNot Applicable

Efficacy of TEAS On Prevention of Propofol Injection Pain in Children

Turkey (Türkiye)60 participantsStarted 2025-02-14

Plain-language 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.

Who can participate

Age range6 Years – 13 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Pain with propofol injection

Timeframe: 5 minutes

Trial details

NCT IDNCT05296187

SponsorKonya Meram State Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-08-26

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