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Completed No phase listed Observational

InSync Implantable Cardioverter Defibrillator Registry: Cardiac Resynchronization Therapy

ClinicalTrials.gov ID: NCT00289302

Public ClinicalTrials.gov record NCT00289302. 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 Jul 22, 2026, 9:46 PM 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
NCT00289302
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Medtronic Cardiac Rhythm and Heart Failure
Industry
Enrollment
600 participants

Conditions and interventions

Interventions

  • Cardiac resynchronization therapy device 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
Dec 31, 2002
Primary completion
Not listed
Completion
Nov 30, 2006
Last update posted
Oct 4, 2007

2003 – 2006

United States locations

U.S. sites
51
U.S. states
32
U.S. cities
51
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Mobile Alabama
Not listed Phoenix Arizona
Not listed San Diego California
Not listed Stanford California
Not listed New Haven Connecticut
Not listed Newark Delaware
Not listed Jacksonville Florida
Not listed Miami Florida
Not listed Orlando Florida
Not listed Palm Beach Gardens Florida
Not listed St. Petersburg Florida
Not listed Atlanta Georgia
Not listed Chicago Illinois
Not listed Oak Lawn Illinois
Not listed Indianapolis Indiana
Not listed Davenport Iowa
Not listed Des Moines Iowa
Not listed Topeka Kansas
Not listed Lexington Kentucky
Not listed Baton Rouge Louisiana
Not listed Houma Louisiana
Not listed New Orleans Louisiana
Not listed Baltimore Maryland
Not listed Boston Massachusetts
Not listed Burlington Massachusetts
Not listed Rochester Minnesota
Not listed St Louis Missouri
Not listed Las Vegas Nevada
Not listed Cherry Hill New Jersey
Not listed Hackensack New Jersey
Not listed Albany New York
Not listed Chapel Hill North Carolina
Not listed Raleigh North Carolina
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Mayfield Heights Ohio
Not listed Oklahoma City Oklahoma
Not listed Erie Pennsylvania
Not listed Lancaster Pennsylvania
Not listed Providence Rhode Island
Not listed Spartanburg South Carolina
Not listed Memphis Tennessee
Not listed Austin Texas
Not listed Dallas Texas
Not listed Salt Lake City Utah
Not listed Richmond Virginia
Not listed Seattle Washington
Not listed Spokane Washington
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 NCT00289302, 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 4, 2007 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00289302 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →