Propofol-ketamine versus midazolam-ketamine for pediatric sedation during endoscopic exam
Not Applicable
Recruiting
- Conditions
- Factors influencing health status and contact with health services
- Registration Number
- KCT0006216
- Lead Sponsor
- Seoul National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 126
Inclusion Criteria
Children aged between 3 and 17 years old who are planned to undergo gastrointestinal endoscopy under monitored anesthesia care
Exclusion Criteria
?Presence of upper respiratory tract infection or pulmonary disease
?Underlying airway compromise such as laryngomalacia, tracheomalacia or subglottic stenosis
?History of hypersensitivity to midazolam, ketamine or propofol
?Presence of allergy to beans or peanuts
?History of seizure attack
?Presence of arrhythmia, tachycardia, or bradycardia
?Decline to enroll from one of the patient's parents or legal guardians
?Other conditions that are regarded as inappropriate for the study
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ength of stay at the postanesthesia care unit;Rate of appearance of any adverse events at the postanesthesia care unit
- Secondary Outcome Measures
Name Time Method Pediatric sedation state scale during the procedure;Modified Aldrete score on arrival at the postanesthesia care unit;Satisfaction of the patient's guardian after discharge from the postanesthesia care unit;Occurrence of adverse events during sedation;Occurrence rate of adverse events during sedation;Proportion of the patients who required rescue ventilation during sedation;Kind of rescue ventilation;Maximal decrement of the mean blood pressure