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ClinicalTrials.gov record
Completed Not applicable Interventional

PREPARE - Primary Prevention Parameters Evaluation

ClinicalTrials.gov ID: NCT00279279

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00279279. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 14, 2026, 6:08 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to test specific device programming in patients without a previous history of a life-threatening, abnormally fast heartbeat who are implanted with a Medtronic ICD (Implantable Cardioconverter Defibrillator) or ICD with CRT (Cardiac Resynchronozation Therapy) device. The information learned from this study could be used to guide physicians in future ICD or CRT device programming.

Study identification

NCT ID
NCT00279279
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
700 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2003 (Type not available)
Primary completion
Not listed
Completion
May 2006 (Type not available)
Last update posted
Oct 26, 2006

2003 – 2006

United States locations

U.S. sites
31
U.S. states
22
U.S. cities
31
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Mesa Arizona — —
Not listed Phoenix Arizona — —
Not listed San Diego California — —
Not listed San Pablo California — —
Not listed Newark Delaware — —
Not listed Fort Lauderdale Florida — —
Not listed Jacksonville Florida — —
Not listed Merrit Island Florida — —
Not listed Columbus Georgia — —
Not listed Maywood Illinois — —
Not listed Rockford Illinois — —
Not listed Topeka Kansas — —
Not listed Portland Maine — —
Not listed Silver Spring Maryland — —
Not listed Takoma Park Maryland — —
Not listed Boston Massachusetts — —
Not listed Royal Oak Michigan — —
Not listed Minneapolis Minnesota — —
Not listed Paterson New Jersey — —
Not listed Buffalo New York — —
Not listed New York New York — —
Not listed Columbus Ohio — —
Not listed Elyria Ohio — —
Not listed Bethlehem Pennsylvania — —
Not listed Lancaster Pennsylvania — —
Not listed Columbia South Carolina — —
Not listed Nashville Tennessee — —
Not listed Amarillo Texas — —
Not listed Kirkland Washington — —
Not listed Morgantown West Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00279279, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 26, 2006 · Synced Nov 14, 2026

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