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Post-extubation Boussignac CPAP System in Adults With Moderate to Severe Obstructive Sleep Apnea

Obstructive Sleep Apnea (OSA) Clinical Trial

Official title:
Use of the Boussignac CPAP System Immediately Following Extubation to Improve Lung Function in Adults With Moderate to Severe Obstructive Sleep Apnea

Clinical Trial Summary

The purpose of this study is to assess the efficacy of the Boussignac positive airway pressure system (a mask) applied immediately following post-operative extubation in improving lung function in patients with obstructive sleep apnea (OSA). Assessments will be done before surgery and then at 1, 2 and 24 hours following extubation and will be compared to standard care for perioperative airway support. The study aims to give a broader and more inclusive picture (than the current literature) in terms of whether the Boussignac CPAP system should be considered for utilization by anesthesiologists caring for surgical patients with OSA.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01877928
Study type Interventional
Source Queen's University
Contact
Status Terminated
Phase N/A
Start date June 2013
Completion date July 2016
View Details
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