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NCT03527862 Clinical Trial

Perioperative Lung Ultrasonography for Fast-track Cardiac Surgery

Pulmonary Complication Clinical Trial

Official title:
The Effect of Perioperative Lung Ultrasonography on Postoperative Outcomes in Children Undergoing Fast-track Cardiac Surgery

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03527862
Other study ID # H1803-123-932
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 8, 2018
Est. completion date December 20, 2022

Study information
Verified date May 2022
Source Seoul National University Hospital
Contact Jin-Tae Kim, MD, PhD
Phone 82-2-2072-3592
Email jintae73@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators evaluate the usefulness of lung ultrasonography in the perioperative period for postoperative outcomes in children undergoing fast track cardiac surgery.

Description:

Some appropriate intervention such as recruitment maneuver, chest tube insertion, or diuretics will be applied depending on lung ultrasound findings.

Recruitment information / eligibility
Status Recruiting
Enrollment 35
Est. completion date December 20, 2022
Est. primary completion date December 20, 2022
Accepts healthy volunteers No
Gender All
Age group N/A to 5 Years
Eligibility Inclusion Criteria: - Children receiving fast track cardiac surgery protocol - = or < 5 years old - Children with acyanotic heart disease Exclusion Criteria: - Previous history of lung resection surgery - Preoperative chest x-ray abnormalities - Postoperative cyanosis

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Treatment according to lung ultrasonography
Appropriate treatment for atelectasis, pleural effusion, pulmonary edema, pneumothorax or pneumonia which are confirmed by lung ultrasonography

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 Postoperative pulmonary complications Pleural effusion, atelectasis, diaphragmatic dysfunction, pulmonary infection, embolism, respiratory failure, aspiration, pneumothorax, chylothorax, bronchospasm Up to postoperative day 5
Secondary Duration of the use of inotropes Duration of the use of inotropes Up to postoperative day 5
Secondary Length of intensive care unit stay Length of intensive care unit stay up to postoperative day 5
Secondary Lung ultrasonography findings Diagnostic lung ultrasonography until 4 hours after surgery
Secondary ABGA result arterial blood gas analysis results within 4 hours after extubation
Secondary Duration of oxygen therapy Up to postoperative day 5
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