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

NCT06218680 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 134

Last updated 2024-01-23

No results posted yet for this study

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

Conditions

  • Emergence Agitation

Interventions

DRUG

Propofol

recieve propofol 0.5 mg/kg intravenously at end of sevoflurane anesthesia

DRUG

Normal saline

recieve propofol 0.5 mg/kg intravenously at end of sevoflurane anesthesia

Sponsors & Collaborators

  • Khon Kaen University

    lead OTHER

Principal Investigators

  • Santhita Pimonbut, M.D. · department of anesthesiology, faculty of medicine, Khonkaen University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
1 Year
Max Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-20
Primary Completion
2025-04-30
Completion
2025-04-30

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06218680 on ClinicalTrials.gov