NCT02025738

Perioperative Management of Patients With Cardiac Implantable Electronic Devices

Perioperative MAnaGement of patieNts With Cardiac Implantable Electronic Devices: Randomized Controlled Pilot Trial (MAGNET Trial)

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 150 (estimated)
• Sponsor: Rambam Health Care Campus · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

Data on the perioperative management of patients cardiac implantable electronic devices (CIEDs) is limited and published guidelines rely mainly on the experience of the cardiologists and anesthesiologists who manage these patients. Depending on the device type and patient's dependency, these guidelines recommend the intraoperative magnet use, reprogramming of devices or no action. Magnet placement on a CIED (very simple and applicable method) has become the standard approach in many centers, while CIED reprograming by trained personnel is required in most centers. Therefore, our objective is to compare in a prospective randomized clinical trial the safety of intraoperative magnet use vs. CIEDS reprogramming vs. no intervention (in the appropriate subjects)

Conditions

• CARDIAC PACEMAKERS DEFIBRILLATOR ELECTROMAGNETIC

Interventions

Type	Name	Description
DEVICE	MAGNET APPLICATION
DEVICE	REPROGRAMING
DEVICE	NO ACTION

Timeline

• Start date: 2014-01-01
• Primary completion: 2015-12-01
• First posted: 2014-01-01
• Last updated: 2015-05-06

Locations

1 site across 1 country: Israel