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Preoxygenation for Difficult Airway Management — PREOPTI-DAM  

Intubation;Difficult Clinical Trial

Official title:
PREOPTI-DAM: High-flow Nasal Cannula Oxygen Versus Standard Oxygenation During Intubation for Patient at Risk of Difficult Intubation: A Randomized Controlled Clinical Trial

Clinical Trial Summary

Tracheal intubation in operating room for patients at risk of difficult intubation remains a critical event. The aim of this study is to determine whether Nasal High Flow Therapy by nasal cannula Optiflow® administered before and during intubation is more efficient than the standard care for pre-oxygenation and oxygenation during anticipated difficult intubation

Clinical Trial Description

This study will be designed as followed: Patients will be randomized in 2 groups: - Preoxygenation during 4 minutes with High Flow Nasal Cannula (60l/min FiO2 = 1) before and during intubation. The device will be maintained in place throughout the intubation procedure (including fiber-optic or laryngoscopic) in order to achieve oxygenation. - Or Standard Preoxygenation during 4 minutes with FIBROXY® (Fiber-optic intubation) or standard facial mask (Laryngoscopic intubation), at FiO2=100%. FIBROXY mask will be maintained in place during the fiberoptic procedure. Standard facial mask, will be removed after the crash induction. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03604120
Study type Interventional
Source Nantes University Hospital
Contact
Status Completed
Phase N/A
Start date September 19, 2018
Completion date March 8, 2021
View Details
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