Ignite Creation Date:
2024-05-06 @ 4:06 PM
Last Modification Date:
2024-10-26 @ 2:04 PM
Study NCT ID:
NCT04879290
Status:
COMPLETED
Last Update Posted:
2021-11-03
First Post:
2021-04-23
Brief Title:
Comparison of Two FiO2 1 or 05 for Tracheal Extubation in Post-anesthesia Care Unit
Sponsor:
University Hospital Caen
Organization:
University Hospital Caen
Study Overview
Official Title:
Comparison of Two FiO2 1 or 05 for Tracheal Extubation in Post-anesthesia Care Unit a Monocentric Randomized Trial
Status:
COMPLETED
Status Verified Date:
2021-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
EXTUBO2
Brief Summary:
The purpose of the study is to assess the optimal fraction of inspired oxygen 05 or 1 for extubation or removal of a supraglottic airway device after general anesthesia
Detailed 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 05 or 1 FiO2
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 05 or 1 FiO2
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None