Sleep Disordered Breathing Clinical Trial
Official title:
Evaluation of Software Enhancements to the Respironics BiPAP autoSV Device Compared to BiPAP S/T Device
This study is being undertaken to collect data from Respironics, Inc's BiPAP autoSV3 and compare with data from Respironics, Inc's BiPAP S/T device, to confirm that the algorithms in the BiPAP autoSV3 device can safely and effectively treat participants experiencing Comp SAS no worse than the BiPAP S/T device. This will be determined using a comparative, randomized design with the participants blinded to the therapy. Additionally, attempts will be made to blind the central scorer(s) with respect to which device is in use.
Primary Hypothesis and end-point:
The use of the BiPAP autoSV3 device in participants with Comp SAS will treat those
participants no worse than when compared to the BiPAP S/T device with respect to:
- Apnea-Hypopnea Index (AHI)
Secondary Hypothesis and end-points:
The use of the BiPAP autoSV3 device in participants with Comp SAS will treat those
participants no worse than the BiPAP S/T device, with respect to:
- Sleep Variables
- REM, NREM and Total Sleep Time (TST) Indices
- Apnea Hypopnea Index (AHI)
- Center Apnea Index(CAI)
- Obstructive Apnea Index (OAI)
- Mixed Apnea Index (MAI)
- Hypopnea Index (HI)
- Sleep Onset Latency (SOL)
- REM Onset Latency (ROL)
- Wake After Sleep Onset (WASO)
- Total Sleep Time (TST)
- Sleep Efficiency (SE %)
- Wake (W), Stages N1,N2,N3 (NREM), and REM (R) sleep (in minutes)
- Wake (W), Stages N1,N2,N3 (NREM), and REM (R) sleep (% TST)
- Arousal Index [total, AH-related, PLM-related, 'spontaneous']
- Nocturnal oxygenation (measured by continuous pulse oximetry during sleep study)
- AHI (REM, NREM and TST) using modified hypopnea rule.
- AHI (REM, NREM and TST) during epochs for which leak is determined to exist within
acceptable limits
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