Clinical Trial

Janus Feasibility Study

Study Description

Janus Feasibility Study

The purpose of this feasibility study is to assess whether an alternative transvenous lead location affects respiration and airway physiology during a commercial remedA"AR System implant procedure.


Locations Selected Location


No pharmaceutical medication involved No pharmaceutical medication involved
Patients and healthy individuals accepted Patients and healthy individuals accepted

Device - Transvenous nerve stimulation

Acute transvenous nerve stimulation during a commercial implant of remedē® System

Additional Information

Official Study Title

Transvenous Nerve Stimulation Study (Janus Study)

Clinical Trial ID


ParticipAid ID