TRANSFORM-HF: ToRsemide compArisoN With furoSemide FORManagement of Heart Failure
Launched by DUKE UNIVERSITY · Sep 26, 2017
Trial Information
Current as of May 21, 2025
Completed
Keywords
ClinConnect Summary
* This study will be a randomized, unblinded, two-arm, multi-center clinical trial of patients with heart failure who are hospitalized. Heart failure need not be the reason for hospitalization. Patients will be randomized 1:1 to either oral torsemide OR oral furosemide prior to hospital discharge. Oral dosing of torsemide compared to furosemide will be 1mg:2mg. The specific loop diuretic dose will be at the discretion of the treating physician with the above noted conversion.
* Trial enrollment occurs before hospital discharge, at the discretion of the healthcare provider.
* As appropriate,...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- 1. Patient hospitalized (≥ 24 hours or over a change in calendar date) with worsening of chronic heart failure, or new diagnosis of heart failure AND meets one of the following criteria:
- • 1. Has a left ventricular ejection fraction (EF) ≤40% within 24 months prior to and including index hospitalization by any method (with most recent value used to determine eligibility)
- • 2. Has an elevated natriuretic peptide level (either NT-pro-B-type natriuretic peptide or B-type natriuretic peptide) during index hospitalization as measured by local laboratory (with most recent value used to determine eligibility)
- • 2. Plan for a daily outpatient oral loop diuretic regimen upon hospital discharge with anticipated need for long-term loop diuretic use
- • 3. ≥ 18 years of age
- • 4. Signed informed consent
- Exclusion Criteria:
- • 1. End-stage renal disease requiring renal replacement therapy
- • 2. Inability or unwillingness to comply with the study requirements
- • 3. History of heart transplant or actively listed for heart transplant
- • 4. Implanted left ventricular assist device or implant anticipated \<3 months
- • 5. Pregnant or nursing women
- • 6. Malignancy or other non-cardiac condition limiting life expectancy to \<12 months
- • 7. Known hypersensitivity to furosemide, torsemide, or related agents
About Duke University
Duke University, a leading academic and research institution located in Durham, North Carolina, is renowned for its commitment to advancing healthcare through innovative clinical research. With a strong emphasis on interdisciplinary collaboration, Duke conducts a wide array of clinical trials aimed at developing cutting-edge therapies and improving patient outcomes across various medical fields. The university's Clinical Research Institute provides comprehensive support for trial design, implementation, and regulatory compliance, ensuring that all research adheres to the highest ethical and scientific standards. Duke’s dedication to translating research findings into effective clinical practices underscores its role as a pivotal contributor to the global medical community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Minneapolis, Minnesota, United States
New York, New York, United States
Chicago, Illinois, United States
New Orleans, Louisiana, United States
Iowa City, Iowa, United States
Saint Louis, Missouri, United States
Abington, Pennsylvania, United States
Maywood, Illinois, United States
Chicago, Illinois, United States
Detroit, Michigan, United States
Manhasset, New York, United States
Dallas, Texas, United States
Norfolk, Virginia, United States
Pomona, New Jersey, United States
Cleveland, Ohio, United States
Fort Lauderdale, Florida, United States
Tucson, Arizona, United States
Indianapolis, Indiana, United States
Ann Arbor, Michigan, United States
Hartford, Connecticut, United States
Murray, Utah, United States
Philadelphia, Pennsylvania, United States
Wilmington, North Carolina, United States
San Francisco, California, United States
Milwaukee, Wisconsin, United States
Honolulu, Hawaii, United States
Stony Brook, New York, United States
Atlanta, Georgia, United States
Cleveland, Ohio, United States
Rapid City, South Dakota, United States
New York, New York, United States
Augusta, Georgia, United States
Greenville, South Carolina, United States
Murray, Utah, United States
Huntsville, Alabama, United States
Salt Lake City, Utah, United States
Gainesville, Florida, United States
Peoria, Illinois, United States
Chapel Hill, North Carolina, United States
Wynnewood, Pennsylvania, United States
Falls Church, Virginia, United States
West Haven, Connecticut, United States
Los Angeles, California, United States
Richmond, Virginia, United States
New Haven, Connecticut, United States
New Orleans, Louisiana, United States
Philadelphia, Pennsylvania, United States
Aurora, Illinois, United States
New York, New York, United States
Alexander City, Alabama, United States
Bloomington, Indiana, United States
Baltimore, Maryland, United States
Rockville, Maryland, United States
Ypsilanti, Michigan, United States
Jackson, Mississippi, United States
Springfield, Missouri, United States
Bronx, New York, United States
Brooklyn, New York, United States
Durham, North Carolina, United States
Matthews, North Carolina, United States
Ephrata, Pennsylvania, United States
Patients applied
Trial Officials
Eric Velazquez, MD
Principal Investigator
Yale University
Robert Mentz, MD
Principal Investigator
Duke University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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