Clinical trial

OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and…

NCT00277524 · Medtronic Cardiac Rhythm and Heart Failure, Industry · Terminated

Key facts

NCT number NCT00277524
Title OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Cardiac Resynchronization Therapy Devices.
Official title OMNI Study--Assessing Therapies in Medtronic Pacemaker, Defibrillator, and Cardiac Resynchronization Therapy Devices.
Acronym OMNI
Lead sponsor Medtronic Cardiac Rhythm and Heart Failure, Industry
Collaborators Medtronic Industry
Status Terminated
Study type Observational
Conditions Tachycardia, Ventricular, Heart Failure, Congestive, Ventricular Fibrillation, Ventricular Dysfunction, Bradycardia
Enrollment 3,032
Start date Aug 1, 2005
Primary completion Nov 1, 2010
Completion Nov 1, 2010
First posted Jan 16, 2006
Last update posted Aug 28, 2013
Countries United States

At a glance

  • 100–999 Study sites
  • Yes Results posted
  • 1–9 Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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