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End-Expiratory Lung Volume in Children Awakening From Propofol Anesthesia

NCT05821114 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2023-04-20

No results posted yet for this study

Summary

The goal of this pilot randomized clinical trial is to test the effects of high flow nasal oxygen and head elevation during awakening from propofol anesthesia in pediatric patients undergoing airway surgery.

The main question\[s\] it aims to answer are:

* High flow oxygen can decrease the occurence of atelectasis during awakening from propofol anesthesia in pediatric patients?
* Head elevation can decrease the occurence of atelectasis during awakening from propofol anesthesia in pediatric patients?

Researchers will compare high flow oxygen vs low flow oxygen group to see if the use of high flow oxygen decrease the occurence of atelectasis during awakening from propofol anesthesia.

And in each group, the patients will be assigned to supine position vs head elevation position to compare the effects of head elevation during awakening from propofol anesthesia.

Conditions

  • Atelectasis, Postoperative Pulmonary

Interventions

OTHER

Head elevation_H

High flow\_Head-elevation

OTHER

Supine_H

High flow\_Supine

OTHER

Head elevation_L

Low flow\_head elevation

OTHER

Supine_L

Low flow\_supine

Sponsors & Collaborators

  • Seoul National University Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
1 Month
Max Age
7 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-04-07
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05821114 on ClinicalTrials.gov