Heart Failure Clinical Trial

RethinQ Study – Evaluating Pacing in Heart Failure Patients

Summary

Patients with heart failure have a pumping action of the ventricles in which one ventricle contracts before the other ventricle. This uncoordinated (unsynchronized) pumping is due to a delay in the stimulation of the left ventricle because of its increased size. Pacing both the right and the left side of the heart (or cardiac resynchronization therapy [CRT]) has been proven to be effective in the treatment of heart failure (HF). Current market-approved devices combine both pacing (CRT) and shocking (implantable cardioverter defibrillator [ICD]) therapy for patients who have severe heart failure and are at risk for developing life-threatening heart rhythms. These devices provide an electrical pacing stimulus to both ventricles and may help the heart contract in a more coordinated way and improve heart failure symptoms.

The investigational portion of this trial involves the implantation of a market-approved CRT implantable cardioverter defibrillator (CRT-D) system in patients who do not meet the current criteria for a CRT implant. In order to receive a CRT-D implant today, patients must have heart failure symptoms, have a weakened heart muscle, and have uncoordinated pumping of the heart. To demonstrate this uncoordinated pumping of the heart, a test (electrocardiogram [ECG]) is done. It is believed that by using a different test (echocardiogram) to measure whether this uncoordinated pumping is present, more patients will be identified that will benefit from CRT-D therapy. This study will look at whether patients identified by using this echocardiogram test show a benefit from having this CRT-D therapy.

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Full Description

1.0 Problem of Interest

Patients with heart failure have a pumping action of the ventricles in which one ventricle contracts before the other ventricle. This uncoordinated (unsynchronized) pumping is due to a delay in the stimulation of the left ventricle because of its increased size. Pacing both the right and the left side of the heart (or cardiac resynchronization therapy [CRT]) has been proven to be effective in the treatment of heart failure. Current market-approved devices combine both pacing (CRT) and shocking (ICD) therapy for patients who have severe heart failure and are at risk for developing life-threatening heart rhythms. These devices provide an electrical pacing stimulus to both ventricles at the same time and may help the heart contract in a more coordinated way and improve heart failure symptoms.

The investigational portion of this trial involves the implantation of a market-approved CRT implantable cardioverter defibrillator (CRT-D) system in patients who do not meet the current criteria for a CRT implant. In order to receive a CRT-D implant today, patients must have heart failure symptoms, have a weakened heart muscle, and have uncoordinated pumping of the heart. To demonstrate this uncoordinated pumping of the heart, a test (ECG) is done. It is believed that by using a different test (echocardiogram) to measure whether this uncoordinated pumping is present, more patients will be identified that will benefit from CRT-D therapy.

2.0 Study Summary

Testing will be performed to determine if patients are eligible for this study. An EKG (electrical tracing of the heart) will be performed. They will be asked to complete a 6- minute hall walk test that will provide information regarding their ability to exercise and conduct daily activities. An echocardiogram with tissue Doppler imaging (ultrasound of the heart) will be performed to determine how the heart muscle contracts. Results of this echocardiogram will determine if patients are eligible to participate in this study.

The device system that will be implanted consists of a St. Jude Medical CRT-D and three pacing leads (insulted wires that carry electrical energy from the device to the heart). One lead is placed in the upper right chamber of the heart (atrium), a second lead is placed in the lower right chamber of the heart (right ventricle) and the third lead is placed within a vein that runs along the outside of the heart and is positioned at a location near the left lower chamber of the heart (left ventricle).

A randomization visit will occur approximately 14 days after implant. Patients will be randomized (like a flip of a coin) to one of two groups. Each patient will have an equal chance of being randomized to either of the two groups. One group will receive cardiac resynchronization treatment (CRT ON) and the other group will not receive cardiac resynchronization treatment (CRT OFF). Patients in the CRT OFF group can receive cardiac resynchronization treatment at 6 months after randomization if the doctor determines that it is appropriate.

Prior to randomization and programming of the device, the following tests will be completed:

Quality of Life Questionnaire - contains 21 questions that provide information as to how heart failure affects the patient's daily life.
EKG
6-Minute Hall.
Cardiopulmonary Exercise Stress Testing (CPX) - measures the amount of oxygen used by your body while exercising on a treadmill and breathing through a special breathing tube
Echocardiogram

Follow-up visits will occur at 3 and 6 months following randomization and every 6 months thereafter until the end of the study. The tests performed at the randomization visit (Quality of Life Questionnaire, EKG, 6 minute hall walk, CPX and echocardiogram) will be repeated at the 6-month follow-up visit. Additionally, each visit will include a review of the patient's condition and current medications and an evaluation of the CRT-D device.

3.0 How Will the Research Advance Scientific Knowledge and/or Human Health?

It is hoped that by pacing both lower chambers of the heart in these patients that they will feel better. They may be able to do more activities with fewer symptoms. In addition, the information gathered in this study will add to the understanding of treatment options for patients with heart failure.

4.0 What is the Current Standard of Care?

Alternative treatments to the St. Jude Medical CRT-D system (includes the left heart lead) currently available include implantation of a standard ICD system and/or treatment with medications.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Have an approved indication for implantation of an ICD.
Have advanced HF with a New York Heart Association (NYHA) Classification of III, despite receiving optimal pharmacological therapy.
Have a stable heart failure medical regimen.
Have a left ventricular ejection fraction (LVEF) <= 35%.
Have evidence of mechanical dyssynchrony as measured by echocardiography using tissue Doppler imaging or M-mode.
Have a QRS duration < 130 ms (present in all ECG leads).
Have the ability to complete exercise stress testing and 6-minute hall walk test, with the only limiting factors being related to cardiac fitness.
Have the ability to independently comprehend and complete a quality of life questionnaire.
Have the ability to provide informed consent for study participation and be willing and able to comply with the prescribed follow-up tests and schedule of evaluations.

Exclusion Criteria:

Have a standard bradycardic indication for pacing.
Have been previously treated with CRT.
Have continuous atrial fibrillation [AF] (continuous is defined as AF lasting > 1 month) within 1 year prior to enrollment or have undergone cardioversion for AF in the past month.
Have the ability to walk > 450 meters during the 6-minute walk test.
Have a NYHA Classification of I, II or IV.
Have symptomatic chronic obstructive pulmonary disease (COPD) as it relates to exercise ability.
Have a classification of Status 1 for cardiac transplantation or consideration for transplantation over the next 6 months.
Have had a recent myocardial infarction, unstable angina or cardiac revascularization (percutaneous transluminal coronary angioplasty [PTCA] or coronary artery bypass graft [CABG]) within 40 days of enrollment.
Have had a recent cerebrovascular accident (CVA) or transient ischemic attack (TIA) within 3 months of enrollment.
Have severe musculoskeletal disorder(s).
Pregnant or planning for pregnancy in the next 6 months.
Currently participating in, or have participated in any clinical investigation within the last 30 days (the only exception being that of a registry trial).
Have a life expectancy of less than 6 months.
Less than 18 years of age.

Study is for people with:

Heart Failure

Phase:

Phase 3

Estimated Enrollment:

250

Study ID:

NCT00132977

Recruitment Status:

Completed

Sponsor:

Abbott Medical Devices

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There are 34 Locations for this study

See Locations Near You

University Hospital University of Alabama at Birmingham
Birmingham Alabama, 35294, United States
Arizona Arrhythmia Consultants
Scottsdale Arizona, 85251, United States
Arkansas Cardiology, PA
Little Rock Arkansas, 72205, United States
Arkansas Heart Hospital
Little Rock Arkansas, 72211, United States
Glendale Memorial Hospital and Medical Center
Glendale California, 91204, United States
Scripps Green Hospital
La Jolla California, 92037, United States
Mercy General Hospital
Sacramento California, 95819, United States
St. Francis Hospital and Medical Center
Hartford Connecticut, 06105, United States
Shands Jacksonville
Jacksonville Florida, 32209, United States
Orlando Regional Medical Center
Orlando Florida, 32806, United States
Emory University
Atlanta Georgia, 30306, United States
Unversity of Chicago
Chicago Illinois, 30322, United States
Loyola University Medical Center
Maywood Illinois, 60153, United States
Iowa Heart Center
Des Moines Iowa, 50314, United States
Central Baptist Hospital
Lexington Kentucky, 40503, United States
Massachusetts General Hospital
Boston Massachusetts, 02114, United States
Baystate Medical Center
Springfield Massachusetts, 01199, United States
St. John Hospital and Medical Center
Detroit Michigan, 48236, United States
Ingham Regional Medical Center
Lansing Michigan, 48910, United States
United Hospital
Saint Paul Minnesota, 55102, United States
Nebraska Heart Institute
Lincoln Nebraska, 68526, United States
Deborah Heart and Lung Center
Browns Mills New Jersey, 08015, United States
New York Presbyterian Hospital/Cornell University
New York New York, 10021, United States
Mount Sinai Hospital
New York New York, 10029, United States
St. Francis Hospital
Roslyn New York, 11576, United States
University Hospitals of Cleveland
Cleveland Ohio, 44106, United States
Cleveland Clinic Foundation
Cleveland Ohio, 44195, United States
The Ohio State University
Columbus Ohio, 43210, United States
Elyria Regional Medical Center
Elyria Ohio, 44035, United States
Hospital of the University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States
Main Line Health Center/Lankenau Hospital
Wynnewood Pennsylvania, 10969, United States
Medical University of Southern California
Charleston South Carolina, 29401, United States
Stern Cardiovascular Center
Germantown Tennessee, 38138, United States
St. Thomas Hospital
Nashville Tennessee, 37205, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Phase:

Phase 3

Estimated Enrollment:

250

Study ID:

NCT00132977

Recruitment Status:

Completed

Sponsor:


Abbott Medical Devices

How clear is this clinincal trial information?

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