CompletedNot Applicable

Modulation of Propofol Injection Pain by Rubbing and Distraction

Egypt135 participantsStarted 2024-10-16

Plain-language summary

This prospective randomized controlled study will be conducted to evaluate the effects of rubbing and distraction on the incidence and severity of propofol injection pain and compare them with the standard intravenous lidocaine method.

Who can participate

Age range18 Years – 65 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: * Patients of either sex * American Society Anesthesiologists physical (ASA) status I-II * age between 18-65 years old * undergoing elective surgeries under general anesthesia using Propofol for anesthetic induction. Exclusion Criteria: * Allergy to experimental drugs * Abuse of alcohol, analgesia, or sedative antidepressant * Difficulty in communication * Chronic pain syndromes, thrombophlebitis, neurological disease, and analgesic administration at the time of the study

What they're measuring

Incidence of propofol injection pain

Timeframe: Pain will be evaluated every 5 seconds during the propofol injection until loss of concioussness. The highest pain score will be recorded

Trial details

NCT IDNCT06643832

SponsorTanta University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-02-17

View on ClinicalTrials.gov More Propofol Injection trials