Evaluation of the efficacy of oxygen therapy and clinical feasibility of high flow nasal cannula during moderate and deep sedation in pediatric patients
Not Applicable
- Conditions
- Not Applicable
- Registration Number
- KCT0006211
- Lead Sponsor
- Seoul National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 258
Inclusion Criteria
1. Children under moderate or deep sedation
2. American Society of Anesthesiologists physical status 1-3
Exclusion Criteria
1. BPD, respiratory distress, respiratory distress or chronic oxygen therapy
2. pneumothorax
3. increased intracranial pressure
4. massive nasal bleeding
5. complete nasal obstruction
6. skull base fracture
7. airway surgery history
8. pulmonary hypertension
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Desaturation (SpO2 =95%)
- Secondary Outcome Measures
Name Time Method Desaturation (SpO2 =90%);Maximum, minimum and average percutaneous CO2 values ;minimum saturation during sedation ;additional treatment due to respiratory adverse event ;Any adverse event related with sedation