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Clinical Trial Summary

The primary purpose of the study is to evaluate if patients with a standard indication for permanent ventricular pacing, left ventricular ejection fraction without limit, or any QRS duration will profit from the prevention of ventricular desynchronisation.


Clinical Trial Description

The study will be performed as a controlled, single-blind, international, multicenter, prospective, randomized, parallel group design. In order to pragmatically examine the effectiveness of biventricular pacing in patients with an indication for ventricular pacing, the study group with biventricular pacing is compared to a control group with standard pacemakers which only allow univentricular (right ventricular) stimulation, as it has been the standard outside of clinical studies until so far. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00187278
Study type Interventional
Source Abbott Medical Devices
Contact
Status Completed
Phase N/A
Start date May 2003
Completion date October 2014

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