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Post Market Clinical Follow-up of CRT-DX Therapy With Lumax 640/740 HF-T — Pre-CRAFT  

Heart Failure Clinical Trial

Official title:
Post Market Clinical Follow-up of CRT-DX Therapy With Lumax 640/740 HF-T

Clinical Trial Summary

The study is designed to collect data of the performance and confirm the safety of the DX (Diagnostic eXtension) functionality in the Lumax 640/470 HF-T in patients with permanent atrial fibrillation and CRT-D indication according to current ESC guidelines. The DX functionality is a feature, which can be activated in the Lumax 640/740 HF-T when connected to the LinoxSMART S DX right ventricular lead. The combination of these devices enable atrial sensing via a sensing dipole in the ventricular lead and therefore reduces the number of implanted leads without sacrificing atrial information. Atrial pacing can not be provided but is not needed in patients with permanent atrial fibrillation.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01930695
Study type Observational
Source Biotronik SE & Co. KG
Contact
Status Completed
Phase
Start date August 2013
Completion date October 2014
View Details
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