Inspire Home Study: Utilization of Home Monitoring During Therapy Optimization in Patients With an Inspire Upper Airway Stimulation System (Comparison of Home Sleep Testing vs. In-lab Polysomnography Testing)

Inclusion Criteria

• •1. Patient is ≥ 22 years of age;
• •2. Patient has been diagnosed with moderate to severe OSA, with a baseline (pre-implant) AHI ≥ 15 based on a qualified sleep study;
• •3. Patient has been implanted with the Inspire UAS System but not yet activated, or has been scheduled for implant of the Inspire UAS System;
• •4. Patient currently owns a SmartPhone and is willing and able to install and use SmartPhone apps (at no cost to patient);
• •5. Patient is willing to utilize study equipment at home including Home Sleep Test (HST) equipment, pulse oximetry equipment, and sleep tracking equipment in accordance with the study protocol;
• •6. Patient is willing and able to return for all follow-up study visits;
• •7. Patient is willing to be randomized and adhere to randomization allocation;
• •8. Patient is willing to and capable of providing informed consent.