Heart Failure Clinical Trial

Clinical Investigation of the Medtronic Concertoâ„¢ Device

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.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Subjects who require the implantation of an Implantable Cardioverter Defibrillator
Subjects who have heart failure that severely limits daily activities (NYHA Class III) or Subjects who have severe heart failure and should always be resting (NYHA Class IV)
Subjects with reduced heart pumping function (left ventricular ejection fraction ≤ 35%)

Exclusion Criteria:

Subjects who have constant atrial fibrillation (top chambers of the heart beat too fast continuously)
Subjects who are post-heart transplant

Study is for people with:

Heart Failure

Estimated Enrollment:

270

Study ID:

NCT00268320

Recruitment Status:

Completed

Sponsor:

Medtronic Cardiac Rhythm and Heart Failure

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There is 1 Location for this study

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Anchorage Alaska, , United States

Phoenix Arizona, , United States

Santa Monica California, , United States

Jacksonville Florida, , United States

Orlando Florida, , United States

Pensacola Florida, , United States

Atlanta Georgia, , United States

Evanston Illinois, , United States

Fort Wayne Indiana, , United States

Des Moines Iowa, , United States

Brighton Massachusetts, , United States

Detroit Michigan, , United States

St. Paul Minnesota, , United States

Kansas City Missouri, , United States

St. Louis Missouri, , United States

Newark New Jersey, , United States

Albuquerque New Mexico, , United States

Syracuse New York, , United States

Cincinnati Ohio, , United States

Cleveland Ohio, , United States

Oklahoma City Oklahoma, , United States

Pittsburgh Pennsylvania, , United States

West Reading Pennsylvania, , United States

Charleston South Carolina, , United States

Nashville Tennessee, , United States

Austin Texas, , United States

Fort Worth Texas, , United States

Richmond Virginia, , United States

Tacoma Washington, , United States

Morgantown West Virginia, , United States

Linz , , Austria

St. Poelten , , Austria

Copenhagen , , Denmark

Aachen , , Germany

Bernau , , Germany

Bochum , , Germany

Goettingen , , Germany

Heidelberg , , Germany

Muenster , , Germany

Patras , , Greece

Negrar Veneto, , Italy

Bologna , , Italy

Tsukuba Ibaraki, , Japan

Suita Osaka, , Japan

Shinjuku-ku Tokyo, , Japan

Eindhoven , , Netherlands

Rotterdam , , Netherlands

Oslo , , Norway

Valencia , , Spain

Basel , , Switzerland

Southhampton , , United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Estimated Enrollment:

270

Study ID:

NCT00268320

Recruitment Status:

Completed

Sponsor:


Medtronic Cardiac Rhythm and Heart Failure

How clear is this clinincal trial information?

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