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Clinical Trial Summary

The goal of X-Change HF is to estimate the effect of biventricular stimulation in patients who need antibradycardia ventricular stimulation (more than 80%); are eligible for the exchange of an old pacemaker or implantable cardioverter defibrillator (ICD); and have ventricular dysfunction (left ventricular ejection fraction [LVEF] < 35%). All patients eligible for participation in the study will be upgraded with a cardiac resynchronization therapy (CRT)-device and receive either right ventricular or biventricular stimulation in a crossover protocol. The endpoint is functional performance measured by spiroergometry.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00157846
Study type Interventional
Source Medtronic Bakken Research Center
Contact
Status Terminated
Phase Phase 4
Start date October 2003
Completion date August 2008

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