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.

Location

Locations Selected Location

Methods

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

NCT03985527

ParticipAid ID

aQW89d