Clinical Trials Directory

Trials / Unknown

UnknownNCT06218680

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

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
134 (estimated)
Sponsor
Khon Kaen University · Academic / Other
Sex
All
Age
1 Year – 8 Years
Healthy volunteers
Not accepted

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

Interventions

TypeNameDescription
DRUGPropofolrecieve propofol 0.5 mg/kg intravenously at end of sevoflurane anesthesia
DRUGNormal salinerecieve propofol 0.5 mg/kg intravenously at end of sevoflurane anesthesia

Timeline

Start date
2024-01-20
Primary completion
2025-04-30
Completion
2025-04-30
First posted
2024-01-23
Last updated
2024-01-23

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT06218680. Inclusion in this directory is not an endorsement.