Enrollment for this study is complete.
Purpose/Detailed Description
Between 3% and 19% of patients with obstructive sleep apnea syndrome (OSA) develop central apneas after application of continuous positive airway pressure (CPAP), a pattern called the complex sleep apnea syndrome (CompSAS). The trial seeks to determine the efficacy of the VPAP™ Adapt SV for the treatment of CompSAS over time.
Maximum time for subject’s participation is 4 months to allow for completion of all tests and exams.
Condition |
Intervention |
Complex sleep apnea syndrome (CompSAS) |
Device: VPAP Adapt SV |
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: CompSAS Resolution Study