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Search / Trial NCT03296813

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

Loop Diuretic

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.

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

0 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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