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Comparison of Two FiO2 (1 or 0.5) for Tracheal Extubation in Post-anesthesia Care Unit — EXTUBO2  

Anesthesia Clinical Trial

Official title:
Comparison of Two FiO2 (1 or 0.5) for Tracheal Extubation in Post-anesthesia Care Unit : a Monocentric Randomized Trial

Clinical Trial Summary

The purpose of the study is to assess the optimal fraction of inspired oxygen (0.5 or 1) for extubation or removal of a supraglottic airway device after general anesthesia.

Clinical Trial Description

During pre-anesthesia visit, eligible patients receive oral and written information of the study and potential risks. In the operating room all patients giving a written informed consent will undergo at the end of surgery a screening to determine eligibility for study entry. Before emergence from general anesthesia, patients who meet the eligibility requirements will be randomized in a open label manner to receive a 0.5 or 1 FiO2. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04879290
Study type Interventional
Source University Hospital, Caen
Contact
Status Completed
Phase N/A
Start date April 9, 2021
Completion date August 16, 2021
View Details
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