A randomized controlled trial using nasal cannula to decrease hypoxia in pediatric patient during rapid sequence intubation compared with control group

Phase 4

Completed

• Conditions: Healthy neonates, infants, and children aged up to 6 years old.Scheduled for elective or emergency surgery under general anesthesia with rapid sequence induction and intubation.; rapid sequence induction and intubation; apnea oxygenation; neonates, infants, and children; nasal cannula

• Registration Number: TCTR20210802002
• Lead Sponsor: Siriraj Research Development Fund, Faculty of Medicine, Siriraj Hospital,Mahidol University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2021-03-02
• Study Start: 2021-08-02
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 64

Inclusion Criteria

1. ASA physical status between 1 to 3
2. Scheduled for elective or emergency surgery under general anesthesia with rapid sequence induction and intubation.

Exclusion Criteria

1. heart disease
2. respiratory problems (either disease or obstruction)
3. history or predicted difficult airway management
4. fever (body temperature more than 37.5 Celsius degree)
5. Allergies to drug use in the study

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
incidence of desaturation q 10 O2 saturation less than 92%

Secondary Outcome Measures

Name	Time	Method
time to desaturation or success intubation q 10 seconds