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NCT00268320 · ClinicalTrials.gov registry record · NA

Clinical Investigation of the Medtronic Concerto™ Device

A NA study, sponsored by Medtronic Cardiac Rhythm and Heart Failure.

Completed
Registry status
NA
Development phase
270
Enrollment target

NCT00268320 is a NA study that has completed, run by Medtronic Cardiac Rhythm and Heart Failure. The registered enrollment target is 270 participants.

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The verdict

NCT00268320, a NA study, has completed, sponsored by Medtronic Cardiac Rhythm and Heart Failure.

COMPLETED
Registry status
NA
Development phase
270 participants
Enrollment target

Study Summary

Heart failure is a progressive disease that decreases the pumping action of the heart. This may cause a backup of fluid in the heart and may result in heart beat changes. When there are changes in the heart beat sometimes an implantable heart device is used to control the rate and rhythm of the heart beat. In certain heart failure cases, when the two lower chambers of the heart no longer beat in a coordinated manner, cardiac resynchronization therapy may be prescribed. People who have a dangerously fast heart beat, or whose heart is at risk of stopping beating, may be in need of an electronic device called an implantable cardioverter defibrillator (ICD). Atrial tachyarrhythmia (AT) is the name for rapid beats in the upper chambers of the heart. People with AT may experience symptoms such as heart palpitations (a racing or pounding feeling in the chest), shortness of breath, dizziness, fatigue or weakness. The purpose of this study is to study an investigational implantable device containing Cardiac Resynchronization Therapy (CRT) and Implantable Cardioverter Defibrillator (ICD) therapies (CRT+ICD device) in subjects who are at significant risk of developing atrial tachyarrhythmias.

Interventions

  • DEVICE Cardiac Resynchronization Therapy+Implantable Cardioverter Defibrillator

Trial Details

FieldValue
Enrollment Target 270 participants
Start Date 2006-01
Est. Completion 2007-07
Phase NA

What the Registry Record Tells You About NCT00268320

The ClinicalTrials.gov registry entry for NCT00268320 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 270 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medtronic Cardiac Rhythm and Heart Failure, which has 115 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Cardiac Resynchronization Therapy+Implantable Cardioverter Defibrillator is the first listed.

NCT00268320 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00268320 about?

NCT00268320 is a clinical study titled "Clinical Investigation of the Medtronic Concerto™ Device". Heart failure is a progressive disease that decreases the pumping action of the heart. This may cause a backup of fluid in the heart and may result in heart beat changes. When there are changes in the heart beat sometimes an implantable heart device is used to control the rate and rhythm of the hear...

What is the current status of trial NCT00268320?

This trial is currently completed. It is a NA study. The enrollment target is 270 participants. The study started on 2006-01. Estimated completion is 2007-07.

What interventions are being tested in trial NCT00268320?

The interventions under investigation include: Cardiac Resynchronization Therapy+Implantable Cardioverter Defibrillator (DEVICE).

Who is sponsoring clinical trial NCT00268320?

This trial is sponsored by Medtronic Cardiac Rhythm and Heart Failure, which has 115 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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