Janus Feasibility Study

Status Recruiting

Clinical Trial Summary

The purpose of this feasibility study is to assess whether an alternative transvenous lead location affects respiration and airway physiology during a commercial remedē® System or commercial transvenous cardiac device (de novo pacemaker or implantable cardiac defibrillator) implant procedure.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Sleep Apnea Syndromes

Clinical Trial Details

NCT number	NCT03985527
Study type	Interventional
Source	Respicardia, Inc.
Contact	Samantha Bruning
Phone	507-226-2953
Email	samantha.bruning@zoll.com
Status	Recruiting
Phase	N/A
Start date	January 9, 2020
Completion date	June 30, 2024

View Details

See also
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