Spinal Cord Stimulation to Treat Post-operative Atrial Fibrillation

NATerminatedINTERVENTIONAL
Enrollment

4

Participants

Timeline

Start Date

February 28, 2015

Primary Completion Date

February 29, 2016

Study Completion Date

February 29, 2016

Conditions
Atrial Fibrillation
Interventions
DEVICE

Spinal Cord Stimulation System

High frequency stimulation using a catheter placed in the lumen of the spine to inhibit sympathetic outflow to the heart

DEVICE

Holter Recording_ NEMon DR220 Holter Recorders

To measure primary endpoint and most of the secondary endpoints in all the patients enrolled in the study. The recording will start to before CABG procedure and will be stop at day 5.

Trial Locations (1)

7511 JX

Medisch Spectrum Twente (MST), Enschede

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Medtronic BRC

INDUSTRY