Comparison of effects of intranasal midazolam and intravenous ketamine for sedation during computed tomography in a pediatric emergency department: a pilot study
Not Applicable
- Conditions
- Not Applicable
- Registration Number
- KCT0008495
- Lead Sponsor
- Seoul National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 34
Inclusion Criteria
Children aged 1 to 5 who visited the pediatric emergency department requiring noncontrast computed tomography under procedural sedation.
Exclusion Criteria
- Children whose American Society of Anesthesiologists physical status classification (ASA) is 3, 4, 5
- Children with suspected otolaryngeal disease or trauma
- Children weighing 20kg or more
- Children with history of previous side effects of sedatives and for whom any of the sedatives were contraindicated.
- Children whose vital signs are unstable or requiring urgent intervention.
- Child's caregiver have insufficient knowlege of Korean to understand the study protocol.
- Intravenous line has already been placed or is planned for a purpose other than procedural sedation.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method success rates of sedation
- Secondary Outcome Measures
Name Time Method Total sedation time ;Induction time;Time to return to baseline ;Sedation depth ;Number of sedatives administered;Dose of sedatives administered ;Adverse events;caregiver satisfaction with sedation