ClinicalTrials.gov record
Completed Not applicable Interventional

Clinical Investigation of the Medtronic Concerto™ Device

ClinicalTrials.gov ID: NCT00268320

Public ClinicalTrials.gov record NCT00268320. 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 May 12, 2026, 7:21 AM EDT

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

Official title

Clinical Investigation of the Medtronic Concerto™ Cardiac Resynchronization Therapy (CRT) and Implantable Cardioverter Defibrillator (ICD) Therapies (CRT+ICD Device)

Study identification

NCT ID
NCT00268320
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Medtronic Cardiac Rhythm and Heart Failure
Industry
Enrollment
270 participants

Conditions and interventions

Interventions

  • Cardiac Resynchronization Therapy+Implantable Cardioverter Defibrillator 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, 2005
Primary completion
May 31, 2006
Completion
Jun 30, 2007
Last update posted
Sep 24, 2008

2006 – 2007

United States locations

U.S. sites
30
U.S. states
24
U.S. cities
30
Facility City State ZIP Site status
Not listed Anchorage Alaska
Not listed Phoenix Arizona
Not listed Santa Monica California
Not listed Jacksonville Florida
Not listed Orlando Florida
Not listed Pensacola Florida
Not listed Atlanta Georgia
Not listed Evanston Illinois
Not listed Fort Wayne Indiana
Not listed Des Moines Iowa
Not listed Brighton Massachusetts
Not listed Detroit Michigan
Not listed Saint Paul Minnesota
Not listed Kansas City Missouri
Not listed St Louis Missouri
Not listed Newark New Jersey
Not listed Albuquerque New Mexico
Not listed Syracuse New York
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Oklahoma City Oklahoma
Not listed Pittsburgh Pennsylvania
Not listed West Reading Pennsylvania
Not listed Charleston South Carolina
Not listed Nashville Tennessee
Not listed Austin Texas
Not listed Fort Worth Texas
Not listed Richmond Virginia
Not listed Tacoma 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 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00268320, 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 Sep 24, 2008 · Synced May 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00268320 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →