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Clinical Trials/NCT00279968
NCT00279968
Completed
N/A

Investigating Significant ICD Heart Therapies Registry Study (INSIGHTS ICD Registry)

Medtronic Cardiac Rhythm and Heart Failure0 sites1,326 target enrollmentFebruary 2004

Overview

Phase
N/A
Intervention
Not specified
Conditions
Ventricular Tachycardia
Sponsor
Medtronic Cardiac Rhythm and Heart Failure
Enrollment
1326
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

The purpose of the Registry is to collect data on how Implantable Cardioverter Defibrillator (ICD) therapies and medications are being used by physicians to treat ventricular arrhythmias in order to better understand how to improve the clinical care of patients and effectiveness of ICD therapies.

Registry
clinicaltrials.gov
Start Date
February 2004
End Date
January 2006
Last Updated
18 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Medtronic Cardiac Rhythm and Heart Failure

Eligibility Criteria

Inclusion Criteria

  • Patients 18 years of age or older.
  • Patients or legal guardians who are willing and able to sign a Permission for Access to and Use of Health Information in a Registry Form and, if required by an Institution's IRB, an Informed Consent.
  • New or replacement implants of Medtronic market released single, dual or triple chamber ICDs including: GEM VR, GEM DR, GEM III AT, Marquis VR, Marquis DR, Maximo DR, Maximo VR, InSync ICD, InSync Marquis ICD and InSync II Marquis ICD.

Exclusion Criteria

  • Patients enrolled in a device study which effects programming and or treatment.

Outcomes

Primary Outcomes

Not specified

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