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

Medtronic

Status: Completed

Conditions: Bradycardia; Pacemaker

Treatments: Device: Pacemaker

Study type: Observational

Funder types: Industry

Identifiers

NCT00294034

197

Details and patient eligibility

About

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.

Full 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.

Sex: All

Volunteers: No Healthy Volunteers

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