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
| Type | Name | Description |
|---|---|---|
| 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 |
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.