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Completed Not applicable Interventional

InSync III Marquis Model 7279 Cardioverter Defibrillator Cardiac Resynchronization System

ClinicalTrials.gov ID: NCT00271232

Public ClinicalTrials.gov record NCT00271232. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 26, 2026, 5:46 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Study identification

NCT ID
NCT00271232
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Medtronic Cardiac Rhythm and Heart Failure
Industry
Enrollment
238 participants

Conditions and interventions

Conditions

Interventions

  • Cardiac resynchronization therapy Device

Device

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
Feb 28, 2003
Primary completion
Not listed
Completion
Mar 31, 2005
Last update posted
Dec 20, 2007

2003 – 2005

United States locations

U.S. sites
34
U.S. states
21
U.S. cities
34
Facility City State ZIP Site status
Not listed Anchorage Alaska
Not listed Phoenix Arizona
Not listed Los Angeles California
Not listed Stanford California
Not listed Jacksonville Florida
Not listed Pensacola Florida
Not listed Tampa Florida
Not listed Atlanta Georgia
Not listed Beech Grove Indiana
Not listed Burlington Massachusetts
Not listed Minneapolis Minnesota
Not listed Saint Paul Minnesota
Not listed Kansas City Missouri
Not listed Lincoln Nebraska
Not listed Las Vegas Nevada
Not listed Lebanon New Hampshire
Not listed New York New York
Not listed Rochester New York
Not listed Syracuse New York
Not listed Raleigh North Carolina
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Lancaster Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Wynnewood Pennsylvania
Not listed Aiken South Carolina
Not listed Columbia South Carolina
Not listed Memphis Tennessee
Not listed Nashville Tennessee
Not listed Austin Texas
Not listed Dallas Texas
Not listed Falls Church Virginia
Not listed Milwaukee Wisconsin

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00271232, 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 Dec 20, 2007 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00271232 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →