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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00294034
First Posted: February 20, 2006
Last Update Posted: March 27, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborators:
Medtronic
Medtronic BRC
Information provided by:
Medtronic Cardiac Rhythm and Heart Failure
  Purpose
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.

Condition Intervention
Pacemaker Bradycardia Device: Pacemaker

Study Type: Observational
Study Design: Observational Model: Defined Population
Observational Model: Natural History
Time Perspective: Longitudinal
Time Perspective: Prospective
Official Title: VIBRANT Registry: Value of Information Based From Pacemaker Recordings and New Technologies

Further study details as provided by Medtronic Cardiac Rhythm and Heart Failure:

Estimated Enrollment: 950
Study Start Date: October 2002
Study Completion Date: May 2006
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.
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00294034


  Show 27 Study Locations
Sponsors and Collaborators
Medtronic Cardiac Rhythm and Heart Failure
Medtronic
Medtronic BRC
Investigators
Principal Investigator: Norman Jaffe, MD Onondaga Hill Cardiovascular Group
Principal Investigator: Luis Caceres, MD Prairie Cardiovascular Consultants
  More Information

ClinicalTrials.gov Identifier: NCT00294034     History of Changes
Other Study ID Numbers: 197
First Submitted: February 16, 2006
First Posted: February 20, 2006
Last Update Posted: March 27, 2007
Last Verified: March 2007

Keywords provided by Medtronic Cardiac Rhythm and Heart Failure:
Registry
Pacemaker
Diagnostics

Additional relevant MeSH terms:
Bradycardia
Arrhythmias, Cardiac
Heart Diseases
Cardiovascular Diseases
Pathologic Processes