VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New Technologies

Completed

• Conditions: Pacemaker; Bradycardia

• Registration Number: NCT00294034
• Lead Sponsor: Medtronic Cardiac Rhythm and Heart Failure

Brief Summary

The purpose of this study is to collect data from pacemakers and determine how this information is used by physicians to care for their patients with pacemakers.

Detailed Description

The purpose of this registry is to gain a better understanding of how diagnostic capabilities in four Vitatron pacemakers (Selection AFm, Clarity, C-Series, and T-Series) are being utilized for the clinical management of a general pacing population. Pacemaker information and health status is collected from all patients enrolled.

Study Timeline

• Study Start: 2002-10
• Study First Submitted: 2006-02-16
• Study First Submitted QC: 2006-02-16
• Study First Posted: 2006-02-20
• Study Completion: 2006-05
• Status Verified: 2007-03
• Last Update Submitted: 2007-03-26
• Last Update Posted: 2007-03-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 950

Inclusion Criteria

• Class I or Class II indication for dual chamber pacing

Exclusion Criteria

• Has an ICD or is a known candidate for an ICD

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified