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OpenTrials
Completed

NCT Number: NCT00294034

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

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.

Completed

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Hot Springs, Arkansas, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

pacemaker

Device

Sponsors and collaborators

Lead sponsor

Medtronic Cardiac Rhythm and Heart Failure

Industry

Collaborators

  • Medtronic
  • Medtronic BRC

Registry information

Important dates

Study start
2002
Study completion
2006
First posted
Feb 20, 2006
Registry last updated
Mar 27, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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