common.study.topics.clinical

Janus Feasibility Study

common.study.values.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.

common.study.values.location

participant.ui.study.affiliations-map.online-study.header-virtual

participant.ui.study.affiliations-map.online-study.text

participant.ui.study.affiliations-map.legend.locations participant.ui.study.affiliations-map.legend.selected

common.study.values.methods

No pharmaceutical medication involved common.study.methods.has-drugs-no
Patients and healthy individuals accepted common.study.methods.is-healthy-no

Device - Transvenous nerve stimulation

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

participant.views.study.view.additional

participant.views.study.view.scientific-title

Transvenous Nerve Stimulation Study (Janus Study)

common.study.values.clinical-trial-id

NCT03985527

participant.views.study.view.id

aQW89d