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

Completed

Conditions studied: Pacemaker, Bradycardia

In brief

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.

Key facts

Study ID

NCT00294034

Run by

Medtronic Cardiac Rhythm and Heart Failure

People needed

950

Starts

2002-10-01

Expected to finish

2006-05-01

Last updated by the study team

2007-03-27

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Class I or Class II indication for dual chamber pacing

You may not qualify if…

• Has an ICD or is a known candidate for an ICD

Where it is running

• Study site — Hot Springs, Arkansas, United States
• Study site — Little Rock, Arkansas, United States
• Study site — North Little Rock, Arkansas, United States
• Study site — Fort Lauderdale, Florida, United States
• Study site — Largo, Florida, United States
• Study site — Ormond Beach, Florida, United States
• Study site — St. Petersburg, Florida, United States
• Study site — Chicago, Illinois, United States
• Study site — Edgewood, Kentucky, United States
• Study site — Louisville, Kentucky, United States
• Study site — Hyannis, Massachusetts, United States
• Study site — Lansing, Michigan, United States
• Study site — Bay Shore, New York, United States
• Study site — Syracuse, New York, United States
• Study site — Bismarck, North Dakota, United States
• Study site — Barberton, Ohio, United States
• Study site — Cincinnati, Ohio, United States
• Study site — Marion, Ohio, United States
• Study site — Massillon, Ohio, United States
• Study site — Middletown, Ohio, United States
• Study site — Pittsburgh, Pennsylvania, United States
• Study site — Columbia, South Carolina, United States
• Study site — Arlington, Texas, United States
• Study site — Austin, Texas, United States
• Study site — Beaumont, Texas, United States

Full record on ClinicalTrials.gov

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