Clinical Trials Directory

Trials / Completed

CompletedNCT01053832

Ventricular Pace Suppression Study

Ventricular Pace Suppression Study With the EVIA/ENTOVIS DR-T/DR Pacemaker

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
84 (estimated)
Sponsor
Biotronik SE & Co. KG · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Investigation of the efficacy and safety of the Ventricular Pace Suppression (VpS) algorithm.

Detailed description

The aim of this study is to investigate the percentage of reduction of ventricular pacing using the VpS feature of the EVIA/ENTOVIS pacemaker in a controlled clinical investigation.

Conditions

Interventions

TypeNameDescription
DEVICEVpS algorithm in EVIA and ENTOVIS pacemakersFor one group of patients, the VpS algorithm will be activated and for the other group, the VpS algorithm will be deactivated until the cross-over, where these conditions will be switched.

Timeline

Start date
2010-01-01
Primary completion
2011-09-01
Completion
2011-09-01
First posted
2010-01-21
Last updated
2011-10-25

Locations

2 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT01053832. Inclusion in this directory is not an endorsement.