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NCT03817177 Clinical Trial

Application of High Flow Nasal Cannula for Prevention of Post-extubation Atelectasis in Children Undergoing Surgery

Atelectasis Clinical Trial

Official title:
Seoul National University Hospital Department of Anesthesiology and Pain Medicine

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03817177
Other study ID # 1812-111-998
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 2, 2019
Est. completion date June 30, 2021

Study information
Verified date March 2019
Source Seoul National University Hospital
Contact Hee-Soo Kim, MD, Phd
Phone 0220723659
Email dami0605@snu.ac.kr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

postoperative atelectasis observation by ultrasound after application of high flow nasal cannula oxygenation

Description:

After surgery, postoperative atelectasis observation by ultrasound grading comparison between application of conventional nasal prong and high flow nasal cannula device

Recruitment information / eligibility
Status Recruiting
Enrollment 80
Est. completion date June 30, 2021
Est. primary completion date January 30, 2021
Accepts healthy volunteers No
Gender All
Age group N/A to 2 Years
Eligibility Inclusion Criteria:

- general anesthesia

Exclusion Criteria:

- preterm

- bronchopulmonary dysplasia

- upper respiratory infection history

- respiratory disease

- cardiac surgery

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• high flow nasal cannula oxygenation
high flow nasal cannula application in PACU
• nasal prong
conventional nasal prong application in PACU

Locations
Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)
Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary lung sound score 0: Normal aeration (N): presence of lung sliding with A lines or fewer than two isolated B lines
Moderate loss of lung aeration: multiple well-defined B lines (B1 lines)
Severe loss of lung aeration: multiple coalescent B lines (B2 lines)
Lung consolidation (C): the presence of a tissue pattern characterized by dynamic air		 30 minutes after arrival of postanesthetic care unit
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