Clinical Trials Logo

Clinical Trial Summary

This investigation is designed to provide supporting evidence for the clinical safety of the Ilesto/Iforia ICD (implantable cardioverter-defibrillator)system and the Evia/Entovis HF-T (Heart Failure) triple chamber pacemaker system when used under specific MRI (magnetic resonance imaging) conditions.


Clinical Trial Description

n/a


Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Safety of MR (Magnetic Resonance) Conditional CRT-pacemakers and ICDs

NCT number NCT01809665
Study type Observational
Source Biotronik SE & Co. KG
Contact
Status Completed
Phase N/A
Start date June 2013
Completion date September 2015