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Safety and Efficacy Study of IPG Patient With Home Monitoring

Bradyarrhythmia Clinical Trial

Official title:
Comparison of the Safety and Efficacy of the Management of Pacemaker Patients Followed-up Via Home Monitoring vs. Conventional In-Office Follow-up

Clinical Trial Summary

The number of patients with implantable pulse generator (IPG) has steadily increased in Japan causing increment in number of in office follow-ups and greater burden on many hospitals. The purpose of this multicenter randomized study is to demonstrate that BIOTRONIK Home Monitoring system reduces office follow-up visits without compromising patient safety.

Clinical Trial Description

Patients will be randomized into HM follow-up only (Group 1) or HM & in-office follow-up (Group 2) and will be followed-up for 27 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01523704
Study type Interventional
Source Biotronik Japan, Inc.
Contact
Status Completed
Phase N/A
Start date January 2012
Completion date February 2016
View Details
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