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NCT03234621 Clinical Trial

Protective Ventilation Strategy

One-lung Ventilation Clinical Trial

Official title:
Protective Ventilation Strategy During One-lung Ventilation: Effect on Postoperative Pulmonary Complications

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03234621
Other study ID # JHBahk_PV
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 12, 2017
Est. completion date January 31, 2018

Study information
Verified date July 2017
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to find a proper ventilation strategy for one-lung ventilation to prevent postoperative pulmonary complications

Recruitment information / eligibility
Status Completed
Enrollment 87
Est. completion date January 31, 2018
Est. primary completion date January 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - patients undergoing elective thoracic surgery - ASA I, II, III - scheduled > 2 hours of surgery Exclusion Criteria: - denied patients - age under 18 years - FEV1/FVC or FEV1<70% in preoperative pulmonary function test

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• ventilator setting during one-lung ventilation
providing various tidal volumes according to the groups with constant PEEP

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 PaO2/FiO2 and/or newly appeared atelectasis, lung infiltration immediately after operation
See also
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