Rapid Assessment of Bedside BNP In Treatment of Heart Failure (RABBIT)
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Purpose
To determine the clinical utility of using the Triage® BNP Test to guide therapy in outpatients with heart failure
| Condition | Intervention | Phase |
|---|---|---|
|
Heart Failure |
Device: Triage® B-Type Natriuretic Peptide (BNP) Test |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single Blind Primary Purpose: Diagnostic |
| Official Title: | Rapid Assessment of Bedside BNP In Treatment of Heart Failure (RABBIT) |
- Combined endpoint of mortality, unplanned clinic or hospital visits that require IV treatment for heart failure, and quality of life.
- All-cause re-hospitalization, Quality of Life, 6 minute walk distance, New York Heart Association class and BNP.
| Estimated Enrollment: | 720 |
| Study Start Date: | July 2003 |
The Triage® BNP Test has been cleared by the U.S. Food and Drug Administration as an aid in the diagnosis and assessment of severity of heart failure. In addition to numerous reports describing the diagnostic and prognostic utility of BNP, reports from various pilot studies have described decreases in BNP in association with various heart failure therapies. Other reports have described modest increases in BNP in association with digitalis and beta-receptor antagonism. The observation that the circulating BNP concentration decreases during heart failure therapy, coupled with the ability of BNP to be used as a prognostic tool and assess the severity of heart failure, it is hypothesized that using BNP measurements to guide heart failure therapy could have a significant impact on the care of heart failure patients. This hypothesis is supported by various reports of pilot studies that describe a significant benefit of administering therapy tailored to concentrations of BNP and related peptides. Patients that are discharged after a hospitalization for heart failure will be approached for study enrollment.This is a multi-center, single (patient)-blinded cluster-randomized study. Half of the sites will have BNP measurements available to guide therapy (experimental arm) and the other half of the sites will not have BNP measurements available (control arm). Blood (plasma) will be collected at each visit and appropriate forms completed. Patients will be asked to complete a Minnesota living with heart failure questionnaire and to do a 6-minute walk test. Patients will be followed for 12 months.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Age 18 or older Patient was hospitalized and treated for heart failure Patient is fully stabilized at discharge Able to give informed consent
Exclusion Criteria:
History of severe pulmonary disease Chronic O2 therapy for COPD Primary pulmonary hypertension History of renal disease requiring dialysis History of severe hepatic disease Patients using LVAD’s Stroke, MI, PTCA, CABG or unstable angina within the past 1 month Bi-ventricular pacemaker placement within last 1 month History of severe aortic stenosis History of severe mitral stenosis History of constrictive pericarditis Patient has had a cardiac transplant Status 1 cardiac transplant candidates ICD or DRG assignment of non-Q wave MI within last 1 month Patient has cor pulmonale A re-hospitalization, death or an IV treatment for heart failure before the first post-discharge visit and/or15) Planned chronic IV treatment.
Contacts and Locations
Hide Study Locations| United States, Arizona | |
| Scottsdale CardiovascularResearch | |
| Scottsdale, Arizona, United States, 85251 | |
| United States, California | |
| San Diego Veterans Administration Hospital | |
| San Diego, California, United States, 92161 | |
| San Francisco Veterans Administration Hospital | |
| San Francisco, California, United States, 94121-1545 | |
| United States, Colorado | |
| Denver Veterans Administration Hospital | |
| Denver, Colorado, United States, 80220 | |
| United States, Florida | |
| Cardiology Associates of Fort Lauderdale | |
| Fort Lauderdale, Florida, United States, 33308 | |
| Shands at the University of Florida | |
| Gainsville, Florida, United States, 32610 | |
| VNH Heart Center Research | |
| Port Charlotte, Florida, United States, 33952 | |
| Heart and Vascular Institute of Florida | |
| St. Petersburg, Florida, United States, 33701 | |
| United States, Illinois | |
| Northwestern University Memorial | |
| Chicago, Illinois, United States, 60611 | |
| Midwest Heart Institute | |
| Lombard, Illinois, United States, 60148 | |
| Advocate Health | |
| Oak Lawn, Illinois, United States, 60453 | |
| United States, Louisiana | |
| Oschner Clinic | |
| New Orleans, Louisiana, United States, 70121 | |
| United States, Massachusetts | |
| University Mass. Memorial Hospital | |
| Worcester, Massachusetts, United States, 06155 | |
| United States, Michigan | |
| Henry Ford Health System | |
| Detroit, Michigan, United States, 48202 | |
| William Beaumont Hospital-Troy | |
| Troy, Michigan, United States, 48085 | |
| United States, Minnesota | |
| Minnesota Veterans Administration | |
| Minneapolis, Minnesota, United States, 55417 | |
| United States, New Jersey | |
| Medicor Cardiology | |
| Bridgewater, New Jersey, United States, 08807 | |
| United States, New York | |
| Buffalo Heart Group, | |
| Buffalo, New York, United States, 14215 | |
| Cardiovascular Medical Associates | |
| Garden City, New York, United States, 11530 | |
| SUNY Upstate Medical University | |
| Syracuse, New York, United States, 13210 | |
| South Bay Cardiovascular Associates | |
| West Islip, New York, United States, 11795 | |
| United States, North Carolina | |
| Carolinas Medical Center/Sanger Clinic | |
| Charlotte, North Carolina, United States, 28203 | |
| Duke University | |
| Durham, North Carolina, United States, 27710 | |
| United States, Ohio | |
| University of Cincinnati | |
| Cincinnati, Ohio, United States, 45267-0542 | |
| Cleveland University Hospital | |
| Cleveland, Ohio, United States, 44106 | |
| Cleveland Clinic Foundation | |
| Cleveland, Ohio, United States, 44106 | |
| United States, Texas | |
| Baylor College of Medicine | |
| Houston, Texas, United States, 77030 | |
| San Antonio VA Medical Center | |
| San Antonio, Texas, United States, 32610 | |
| United States, Utah | |
| Latter Day Saints Hospital | |
| Salt Lake City, Utah, United States, 84143 | |
| Principal Investigator: | James B Young, MD | The Cleveland Clinic |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00206856 History of Changes |
| Other Study ID Numbers: | 001 |
| Study First Received: | September 13, 2005 |
| Last Updated: | April 26, 2006 |
| Health Authority: | United States: Food and Drug Administration |
Additional relevant MeSH terms:
|
Heart Failure Heart Diseases Cardiovascular Diseases Natriuretic Peptide, Brain Natriuretic Agents |
Physiological Effects of Drugs Pharmacologic Actions Cardiovascular Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on June 18, 2013