Reducing Decompensation Events Utilizing Intracardiac Pressures in Patients With Chronic Heart Failure (HF) (REDUCEhf)

Completed · Not applicable

Conditions studied: Heart Failure

In brief

The purpose of this clinical research study is to evaluate the safety and effectiveness of the investigational implantable hemodynamic monitor (IHM), and of the IHM in combination with an implantable cardioverter defibrillator (ICD). The investigational IHM has the ability to record and report the force with which the heart pumps blood (heart pressures). When combined with the ICD, the device has the additional ability to send a strong electrical impulse, or shock, to the heart when it detects dangerously fast heartbeats to return it to a normal rhythm. The IHM and IHM/ICD are implanted surgically just under the skin in the upper chest area. This study will also determine how doctors use the information related to heart pressures in the management of heart failure.

Key facts

Study ID

NCT00354159

Run by

Medtronic Cardiac Rhythm and Heart Failure

People needed

442

Starts

2006-04-01

Expected to finish

2011-01-01

Last updated by the study team

2012-08-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects with heart failure that only sometimes interferes with daily activities (New York Heart Association [NYHA] Class II (1)) or subjects with heart failure which severely limits daily activities (NYHA Class III (2)) at baseline
• Subject has appropriate medical therapy for heart failure (such as diuretic, angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) and beta blocker) for at least three months prior to the baseline evaluation.
• Subject has been on stable medications maximized to the subject's tolerance of ACE or ARB and beta blockers as determined by the study investigator for at least 30 days prior to baseline evaluation. (Stable is defined as no more than a 100% increase or a 50% decrease in dose.) If a subject is intolerant of ACE, ARB or beta blockers documented evidence must be available.
• Subject has had at least one heart failure-related hospitalization or at least one heart failure-related emergency department or urgent care visit necessitating heart failure-related intravenous therapy (e.g. diuretic administration) within 12 months prior to the baseline evaluation
• To be considered for Chronicle ICD: Subject has, or is at risk of having, a heart beat that is too fast and his/her doctor has determined he/she needs an implantable cardioverter defibrillator (ICD).
• Class II Subjects with cardiac disease resulting in slight limitation of physical activity. They are comfortable at rest. Ordinary physical activity results in fatigue, palpitation, dyspnea, or angina.
• Class III Subjects with cardiac disease resulting in marked limitation of physical activity. They are comfortable at rest. Less than ordinary activity causes fatigue, palpitation, dyspnea, or angina.

You may not qualify if…

• Subjects with severe heart failure who should always be resting (NYHA Class IV(3)) or Stage D(4) refractory heart failure.
• Subjects with severe renal dysfunction.
• Subjects with severe non-cardiac condition limiting 12-month survival.
• Subjects in concurrent studies that may confound the results.
• (3)Class IV Subjects with cardiac disease resulting in inability to carry on any physical activity without discomfort. Symptoms of heart failure or the anginal syndrome may be present even at rest. If any physical activity is undertaken, discomfort is increased.
• (4)Stage D refractory heart failure: Patients who have marked symptoms at rest despite maximal medical therapy (e.g., those who are recurrently hospitalized or cannot be safely discharged from the hospital without specialized interventions)

Where it is running

• Scripps Green Hospital — La Jolla, California, United States
• Loma Linda University Medical Center — Loma Linda, California, United States
• Long Beach Memorial — Long Beach, California, United States
• Cedars-Sinai Medical Center — Los Angeles, California, United States
• Doctors Medical Center Modesto — Modesto, California, United States
• Yale University, School of Medicine — New Haven, Connecticut, United States
• Christiana Care Hospital — Newark, Delaware, United States
• University of FL Shands — Gainesville, Florida, United States
• Mayo Clinic Jacksonville — Jacksonville, Florida, United States
• Crawford Long/Emory University Hospitals — Atlanta, Georgia, United States
• Midwest Heart Foundation — Lombard, Illinois, United States
• Genesis Hospital Midwest Cardiovascular Research Foundation — Davenport, Iowa, United States
• Iowa Heart Center — West Des Moines, Iowa, United States
• Brigham & Women's Hospital — Boston, Massachusetts, United States
• Lahey Clinic Medical Center — Burlington, Massachusetts, United States
• University of Massachusetts Memorial Medical Center — Worcester, Massachusetts, United States
• St Joseph Mercy Hospital — Ann Arbor, Michigan, United States
• University of Michigan — Ann Arbor, Michigan, United States
• Henry Ford Hospital — Detroit, Michigan, United States
• Mercy Hospital Metropolitan Cardiology Consultants — Coon Rapids, Minnesota, United States
• North Mississippi Medical Center — Tupelo, Mississippi, United States
• Mid America Heart Institute/St. Lukes — Kansas City, Missouri, United States
• Washington University School of Medicine — St Louis, Missouri, United States
• Bryan LGH Heart Institute — Lincoln, Nebraska, United States
• University of Alabama at Birmingham (UAB) — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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