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Comparison Study Using APAP With and Without SensAwake in Patients With OSA and PTSD

Obstructive Sleep Apnea (OSA) Clinical Trial

Official title:
Comparison Study Using APAP With and Without SensAwake in Patients With OSA and PTSD

Clinical Trial Summary

The purpose of this research is to examine the application of AutoCPAP with and without SensAwake in subjects with OSA and Post-Traumatic Stress Disorder (PTSD), and evaluate whether patients achieve better sleep quality and compliance with SensAwake, compared to the same treatment without SensAwake.

Clinical Trial Description

Conceptually, awareness of pressure occurs only during wakefulness. Thus reducing the pressure during wakefulness may improve therapy comfort and potentially adherence without compromising therapy efficacy. SensAwake™ is a unique pressure relief technology developed by Fisher & Paykel Healthcare which detects irregularity in the flow signal indicative of the transition from sleep to wake. When the transition from sleep to wake is detected the device promptly reduces the pressure to help facilitate a return to sleep. It is hypothesised that AutoCPAP with SensAwake will improve patient comfort and compliance in the PTSD and OSA patients who are naïve to CPAP therapy. The investigators will not be blinded to the study. The participants will be blinded to the study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02549508
Study type Interventional
Source Fisher and Paykel Healthcare
Contact
Status Completed
Phase N/A
Start date October 2015
Completion date May 2018
View Details
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