This study will investigate the efficacy of the FPH modified positive airway pressure (PAP) device with or without SensAwake; and with different pressure support in OSA participants; in both an in-home and in-lab environment. Comfort, compliance and the accuracy of the pressure delivery will also be evaluated. The FPH device will be compared to a market released product.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
29
FPH Device with SensAwake On + Pressure Support A
FPH Device with SensAwake Off + Pressure Support A
FPH Device with SensAwake On + Pressure Support B
Fisher & Paykel Healthcare
Auckland, New Zealand
WellSleep Centre
Wellington, New Zealand
Apnea Hypopnea Index (AHI)
Through the device and independent flow logger
Time frame: 3 nights
Apnea Hypopnea Index (AHI)
Through the polysomnography
Time frame: 1 night
Therapy Comfort
Through a subjective questionnaire
Time frame: 3 nights
Compliance
Through the device and independent flow logger
Time frame: 3 nights
Device Triggering
Through the device
Time frame: 3 nights
Device Triggering
Through the polysomnography
Time frame: 1 night
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FPH Device with SensAwake Off + Pressure Support B
Competitor's PAP Released Device + Pressure Support A
Competitor's PAP Released Device + Pressure Support B