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

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 June 2021

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