LIFE Study - Limiting Chronotropic Incompetence for Pacemaker Recipients

Status Completed

Clinical Trial Summary

This study will compare how two different sensors inside the pacemaker may affect patients' quality of life.

Clinical Trial Description

The LIFE Study will estimate the prevalence of CI among a general sample of pacemaker patients and compare changes in quality of life and physical activity between patients randomized to receive rate response driven by either blended sensor or accelerometer. Changes in chronotropic response between CI patients randomized to either blended sensor or accelerometer will be compared. A sub-study will evaluate changes in functional capacity between CI patients randomized to either blended sensor or accelerometer. ;

Study Design

Related Conditions & MeSH terms

Bradycardia

Clinical Trial Details

NCT number	NCT00146861
Study type	Interventional
Source	Boston Scientific Corporation
Contact
Status	Completed
Phase	Phase 4
Start date	July 2003
Completion date	January 2006

View Details

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