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

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00294034

Enrollment

950

Registered

2006-02-20

Start date

2002-10-31

Completion date

2006-05-31

Last updated

2007-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bradycardia, Pacemaker

Keywords

Registry, Pacemaker, Diagnostics

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.

Interventions

DEVICEPacemaker

Study design

Observational model

DEFINED_POPULATION

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026