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Clinical Trial Summary

This study is a prospective observer blinded, central randomization controlled, multi-center clinical trial to assess the relationship between intraoperative FiO2 and postoperative pulmonary complications with lung injury.


Clinical Trial Description

Hyperoxia is common in cardiac surgery and is easy to prevent by adjusting FiO2. Since there is no prospective study on different FiO2 and postoperative pulmonary complications (PPCs) during cardiac surgery. We hypothesized that hyperoxia during cardiac surgery could lead to higher incidence of lung injury and PPCs than normoxia. The objective of this trial is to compare postoperative PPCs and other outcomes between hyperoxia and normoxia strategy by PaO2/FiO2 in CABG patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04115501
Study type Interventional
Source University of Louisville
Contact
Status Withdrawn
Phase N/A
Start date February 27, 2021
Completion date February 1, 2024

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