RecruitingSleep Apnea
Janus II Feasibility
Eligible age
22+ yrs
Accepts
All genders
Locations
3 states
Healthy volunteers
No
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About this study
The objectives of this study are to evaluate the feasibility of the remedē® Dual Channel System at implant and overnight sleep studies and to assess chronic safety.
Sponsor: Zoll Medical Corporation
You may qualify if…
- ✓ Severe sleep disordered breathing
- ✓ Expected to tolerate study procedures
- ✓ No heart failure or medically stable heart failure
You may not qualify if…
- ✕ Currently implanted with a neurostimulator to treat sleep disordered breathing without sponsor approval
- ✕ History of severe COPD or pulmonary arterial hypertension
- ✕ Current or previous history of nerve injury or palsy
- ✕ Prior cervical surgeries or radiation treatment to head region
- ✕ Known need for an MRI
- ✕ History of psychosis or severe bipolar disorder
- ✕ Active Infection or sepsis within 30 days of enrollment
- ✕ Currently on kidney dialysis or significantly reduced kidney function
Where it's recruiting
Source: ClinicalTrials.gov · NCT06556693 · last updated 2025-10-29