MAVRIC VR ICD Registry

December 20, 2023 updated by: Medtronic Cardiac Rhythm and Heart Failure

Marquis/Maximo VR ICD Programming Practices Registry (MAVRIC VR ICD Registry)

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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment

742

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Canada
    • Alberta
      • Edmonton, Alberta, Canada
    • British Columbia
      • Victoria, British Columbia, Canada
    • Newfoundland and Labrador
      • St. John's, Newfoundland and Labrador, Canada
    • Nova Scotia
      • Halifax, Nova Scotia, Canada
    • Ontario
      • Kingston, Ontario, Canada
      • London, Ontario, Canada
      • Ottawa, Ontario, Canada
      • Toronto, Ontario, Canada
    • Quebec
      • Montreal, Quebec, Canada
      • Ste-Foy, Quebec, Canada
  • United States
    • Alabama
      • Birmingham, Alabama, United States
      • Tuscaloosa, Alabama, United States
    • Arkansas
      • Little Rock, Arkansas, United States
    • California
      • Bakersfield, California, United States
      • Banning, California, United States
      • Fresno, California, United States
      • Mission Viejo, California, United States
      • Sacramento, California, United States
      • San Diego, California, United States
      • Stanford, California, United States
    • Colorado
      • Littleton, Colorado, United States
    • Delaware
      • Newark, Delaware, United States
    • District of Columbia
      • Washington, District of Columbia, United States
    • Florida
      • Jacksonville, Florida, United States
      • Lakeland, Florida, United States
      • Miami Beach, Florida, United States
      • Port Charlotte, Florida, United States
      • Saint Petersburg, Florida, United States
    • Georgia
      • Atlanta, Georgia, United States
      • Augusta, Georgia, United States
      • Decatur, Georgia, United States
    • Illinois
      • Chicago, Illinois, United States
    • Indiana
      • Hobart, Indiana, United States
      • Indianapolis, Indiana, United States
    • Iowa
      • Cedar Rapids, Iowa, United States
      • Davenport, Iowa, United States
    • Kansas
      • Kansas City, Kansas, United States
    • Kentucky
      • Lexington, Kentucky, United States
      • Owensboro, Kentucky, United States
    • Louisiana
      • Marrero, Louisiana, United States
    • Maryland
      • Baltimore, Maryland, United States
      • Salisbury, Maryland, United States
    • Massachusetts
      • Worcester, Massachusetts, United States
    • Michigan
      • Ann Arbor, Michigan, United States
      • Saint Joseph, Michigan, United States
      • Southfield, Michigan, United States
    • Minnesota
      • Coon Rapids, Minnesota, United States
      • Saint Cloud, Minnesota, United States
    • Mississippi
      • Jackson, Mississippi, United States
    • Missouri
      • Cape Girardeau, Missouri, United States
      • Joplin, Missouri, United States
      • Kansas City, Missouri, United States
      • Saint Louis, Missouri, United States
    • Montana
      • Missoula, Montana, United States
    • Nevada
      • Las Vegas, Nevada, United States
    • New Hampshire
      • Lebanon, New Hampshire, United States
    • New Jersey
      • Englewood, New Jersey, United States
    • New York
      • Albany, New York, United States
      • Huntington, New York, United States
      • New Hyde Park, New York, United States
      • New York, New York, United States
      • Syracuse, New York, United States
    • North Carolina
      • Pinehurst, North Carolina, United States
      • Winston-Salem, North Carolina, United States
    • Ohio
      • Cincinnati, Ohio, United States
      • Cleveland, Ohio, United States
      • Columbus, Ohio, United States
      • Mayfield Hts, Ohio, United States
      • Youngstown, Ohio, United States
    • Oklahoma
      • Oklahoma City, Oklahoma, United States
      • Tulsa, Oklahoma, United States
    • Oregon
      • Eugene, Oregon, United States
      • Portland, Oregon, United States
    • Pennsylvania
      • Allentown, Pennsylvania, United States
      • Hershey, Pennsylvania, United States
      • Philadelphia, Pennsylvania, United States
      • Pittsburgh, Pennsylvania, United States
    • South Carolina
      • Spartanburg, South Carolina, United States
    • Tennessee
      • Chattanooga, Tennessee, United States
      • Knoxville, Tennessee, United States
      • Memphis, Tennessee, United States
    • Texas
      • Corpus Christi, Texas, United States
      • Dallas, Texas, United States
      • Fort Worth, Texas, United States
      • Houston, Texas, United States
      • Odessa, Texas, United States
      • Tyler, Texas, United States
    • Virginia
      • Charlottesville, Virginia, United States
      • Richmond, Virginia, United States
    • Washington
      • Tacoma, Washington, United States
    • Wisconsin
      • Milwaukee, Wisconsin, United States

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Medtronic Cardiac Rhythm and Heart Failure

Collaborators

Medtronic

Investigators

  • Principal Investigator: George Klein, M.D., London H.S.C. University Campus

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2004

Study Completion

December 1, 2005

Study Registration Dates

First Submitted

December 28, 2005

First Submitted That Met QC Criteria

December 28, 2005

First Posted (Estimated)

December 29, 2005

Study Record Updates

Last Update Posted (Estimated)

December 21, 2023

Last Update Submitted That Met QC Criteria

December 20, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 232

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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