We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

MAVRIC VR ICD Registry

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00270933
First Posted: December 29, 2005
Last Update Posted: December 28, 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.
Collaborator:
Medtronic
Information provided by:
Medtronic Cardiac Rhythm and Heart Failure
  Purpose
The purpose of this registry is to collect information on the health status of patients receiving Marquis/Maximo VR Implantable Cardiac Defibrillators (ICDs), how the devices are being programmed and how this correlates to clinical patient outcome.

Condition Intervention
Ventricular Tachycardia Ventricular Fibrillation Device: Registry

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Marquis/Maximo VR ICD Programming Practices Registry (MAVRIC VR ICD Registry)

Resource links provided by NLM:


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

Estimated Enrollment: 742
Study Start Date: January 2004
Estimated Study Completion Date: December 2005
  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:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients 18 years of age or older
  • Patients implanted with a new or replacement Marquis VR or Maximo VR ICD

Exclusion Criteria:

  • Patients enrolled in a device study that affects treatment and/or programming
  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): NCT00270933


  Show 91 Study Locations
Sponsors and Collaborators
Medtronic Cardiac Rhythm and Heart Failure
Medtronic
Investigators
Principal Investigator: George Klein, M.D. London H.S.C. University Campus
  More Information

ClinicalTrials.gov Identifier: NCT00270933     History of Changes
Other Study ID Numbers: 232
First Submitted: December 28, 2005
First Posted: December 29, 2005
Last Update Posted: December 28, 2007
Last Verified: December 2007

Keywords provided by Medtronic Cardiac Rhythm and Heart Failure:
defibrillators
LLECG
ventricular tachycardia
ventricular fibrillation

Additional relevant MeSH terms:
Tachycardia
Tachycardia, Ventricular
Ventricular Fibrillation
Arrhythmias, Cardiac
Heart Diseases
Cardiovascular Diseases
Pathologic Processes