Obstructive Sleep Apnea Clinical Trial
Official title:
Effectiveness of Adaptive Servoventilation (ASV) in Patients With Central Sleep Apnea Due to Chronic Opioid Use
Prospective, randomized, blinded, cross-over study assessing the effectiveness of adaptive servo-ventilation (ASV) in treating patients who have obstructive sleep apnea (OSA) complicated by central sleep apnea (CSA) due to the chronic use of opioid medications
The trial seeks to determine the efficacy and patient comfort of ASV and bi-level positive
airway pressure (PAP) modes for the treatment of obstructive sleep apnea (OSA), complicated
by CSA secondary to opioid use. Subjects will be randomized to one of two groups, utilizing
a cross-over design to evaluate the two modes with the subject as their own control.
Subjects will be asked to undergo two PSG studies; one with ASV titration and one with
bi-level treatment, using the current pressure prescription. The study comprises two visits.
Subjects will be asked to complete patient satisfaction questionnaires following their PSG
studies. It is anticipated that total subject participation will be no longer than one
month.
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