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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03453762
Other study ID # H1802-058-921
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 23, 2018
Est. completion date March 1, 2019

Study information

Verified date May 2019
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators compare the degree of atelectasis in recovery room between conventional recruitment maneuver and ultrasonography-guided lung recruitment during surgery.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date March 1, 2019
Est. primary completion date February 20, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 6 Years
Eligibility Inclusion Criteria:

- Patients who undergo surgery for more than 1 hour under general anesthesia

- Children under 6 years old

- American Society of Anesthesiologist Physical Status I or II

Exclusion Criteria:

- History of lung surgery

- Abnormal findings in chest x-ray

- Laparoscopic surgery

- Abdominal surgery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
recruitment maneuver
Recruitment maneuver is provided with positive pressure of 30 cmH2O for 10 seconds.
ultrasonography-guided recruitment maneuver
Recruitment maneuver is guided by 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 Incidence of postoperative atelectasis Postoperative atelectasis is measured using lung ultrasonography within 1 hour after the end of surgery
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