UnknownNot Applicable

Efficacy of Low Dose Propofol Given at the End of Sevoflurane Anesthesia for Prevention of Emergence Agitation in Pediatric Patient Undergoing MRI Scan

Thailand134 participantsStarted 2024-01-20

Plain-language summary

The goal of this clinical trial is to compare Efficacy of low dose propofol(0.5 mg/kg) vs placebo given at the end of sevoflurane anesthesia for prevention of emergence agitation in pediatric patient undergoing MRI scan. The main question it aims to answer is "Can low dose propofol reduce the incidence of emergence agitation after general anesthesia?" Participants will be given propofol 0.5 mg/kg or saline according to the allocated group at the completion of MRI scan

Who can participate

Age range1 Year – 8 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: * Age 2-8 years * ASA class I or II ,who schedule for MRI scan under sevoflurane anesthesia Exclusion Criteria: * Developmental delay * Psychological and neurological disorders * Abnormal airway * Reactive airway disease * Allergy to propofol, egg product * Family history of malignant hyperthermia * Need iv sedative medication before induction * Obesity

What they're measuring

incidence of emergence agitation

Timeframe: at 5,10,15,20,25,30 minutes after extubation

Trial details

NCT IDNCT06218680

SponsorKhon Kaen University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-04-30

Contact for this trial

Santhita Pimonbut, M.D.

66943624641 Santhita.p@kkumail.com

View on ClinicalTrials.gov More Emergence Agitation trials