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Clinical trialNCT00132977CompletedPhase 3Interventional

RethinQ Study - Evaluating Pacing in Heart Failure Patients

SponsorAbbott Medical DevicesEnrollment250Heart Failure
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

34 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • University Hospital University of Alabama at Birmingham

    Birmingham, Alabama, United States

  • Arizona Arrhythmia Consultants

    Scottsdale, Arizona, United States

  • Arkansas Cardiology, Pa

    Little Rock, Arkansas, United States

  • Arkansas Heart Hospital

    Little Rock, Arkansas, United States

  • Glendale Memorial Hospital and Medical Center

    Glendale, California, United States

  • Scripps Green Hospital

    La Jolla, California, United States

  • Mercy General Hospital

    Sacramento, California, United States

  • St. Francis Hospital and Medical Center

    Hartford, Connecticut, United States

  • Shands Jacksonville

    Jacksonville, Florida, United States

  • Orlando Regional Medical Center

    Orlando, Florida, United States

  • Emory University

    Atlanta, Georgia, United States

  • Unversity of Chicago

    Chicago, Illinois, United States

  • Loyola University Medical Center

    Maywood, Illinois, United States

  • Iowa Heart Center

    Des Moines, Iowa, United States

  • Central Baptist Hospital

    Lexington, Kentucky, United States

  • Massachusetts General Hospital

    Boston, Massachusetts, United States

  • Baystate Medical Center

    Springfield, Massachusetts, United States

  • St. John Hospital and Medical Center

    Detroit, Michigan, United States

  • Ingham Regional Medical Center

    Lansing, Michigan, United States

  • United Hospital

    Saint Paul, Minnesota, United States

  • Nebraska Heart Institute

    Lincoln, Nebraska, United States

  • Deborah Heart and Lung Center

    Browns Mills, New Jersey, United States

  • Mount Sinai Hospital

    New York, New York, United States

  • New York Presbyterian Hospital/cornell University

    New York, New York, United States

  • St. Francis Hospital

    Roslyn, New York, United States

  • Cleveland Clinic Foundation

    Cleveland, Ohio, United States

  • University Hospitals of Cleveland

    Cleveland, Ohio, United States

  • the Ohio State University

    Columbus, Ohio, United States

  • Elyria Regional Medical Center

    Elyria, Ohio, United States

  • Hospital of the University of Pennsylvania

    Philadelphia, Pennsylvania, United States

  • Main Line Health Center/lankenau Hospital

    Wynnewood, Pennsylvania, United States

  • Medical University of Southern California

    Charleston, South Carolina, United States

  • Stern Cardiovascular Center

    Germantown, Tennessee, United States

  • St. Thomas Hospital

    Nashville, Tennessee, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Jul 2005
Primary completion
31 Jul 2007
Completion
31 Jul 2007
Last update posted
4 Feb 2019
Registered enrollment
250
Registry id
NCT00132977

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.