Status:

NOT_YET_RECRUITING

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

Lead Sponsor:

Khon Kaen University

Conditions:

Emergence Agitation

Eligibility:

All Genders

1-8 years

Phase:

NA

Brief 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 ...

Eligibility Criteria

Inclusion

  • Age 2-8 years
  • ASA class I or II ,who schedule for MRI scan under sevoflurane anesthesia

Exclusion

  • 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

Key Trial Info

Start Date :

January 20 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

April 30 2025

Estimated Enrollment :

134 Patients enrolled

Trial Details

Trial ID

NCT06218680

Start Date

January 20 2024

End Date

April 30 2025

Last Update

January 23 2024

Active Locations (1)

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1

Khon kaen University

Khon Kaen, Muang, Thailand, 40002

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