RF Surgical Sponge-Detecting System on the Function of Pacemakers and Implantable Cardioverter Defibrillators

NACompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

March 31, 2014

Primary Completion Date

March 31, 2015

Study Completion Date

May 31, 2015

Conditions
CardiomyopathyCardiac ArrhythmiaHeart FailureChronic Thromboembolic Pulmonary Hypertension
Interventions
DEVICE

RF Assure Scanning

CIED and temporary pacemaker patients will be scanned with RF surgical sponge detection wand and mat as well as with and without the RF sponge. The scanning will only be conducted on the device scheduled for removal. Patients will have device interrogated before and after scanning (for CIEDs) to determine if there have been any clinically significant changes in programming or settings due to scanning with RF technology. Vitals will be monitored and recorded before, during, and after scanning.

Trial Locations (1)

92093

UCSD Sulpizio Cardiovascular Center, La Jolla

All Listed Sponsors
collaborator

RF Surgical Systems, Inc.

INDUSTRY

lead

University of California, San Diego

OTHER

NCT02111980 - RF Surgical Sponge-Detecting System on the Function of Pacemakers and Implantable Cardioverter Defibrillators | Biotech Hunter | Biotech Hunter