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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00270933
Other study ID # 232
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2004
Est. completion date December 2005

Study information

Verified date December 2023
Source Medtronic Cardiac Rhythm and Heart Failure
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 742
Est. completion date December 2005
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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 Design


Intervention

Device:
Registry


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Medtronic Cardiac Rhythm and Heart Failure Medtronic

Countries where clinical trial is conducted

United States,  Canada, 

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