Overview
The purpose of this multi-center proof-of-concept safety and efficacy study is to collect chronic sleep-related data following percutaneous placement of electrode arrays near the hypoglossal nerve and the ansa cervicalis in adults with obstructive sleep apnea.
Eligibility
Inclusion Criteria:
- Body Mass Index (BMI) ≤ 32 kg/m2
- AHI between 15-65 events/hour
- Participants who have either not tolerated, have failed or refused positive airway pressure (PAP)
Exclusion Criteria:
- Pregnancy or breast-feeding
- Significant upper airway anatomic abnormalities
- Significant positionally-dependent OSA
- Participants taking medications that may alter body weight