Empagliflozin for Heart Transplant Recipients

This study is looking at whether empagliflozin, a medication, can help heart transplant recipients. After a heart transplant, people can be at higher risk for kidney and heart problems. Empagliflozin has shown benefits for kidney and heart health in other groups of patients. This study will compare empagliflozin to a placebo (an inactive pill) over 12 months to see if it can help improve kidney health, specifically by looking at a marker in your urine called UACR (Urinary albumin-to-creatinine ratio). Researchers will also monitor for any side effects. You may be able to join if you are 18 or older, had a heart transplant at least 3 months ago, and meet other health requirements. The study plans to enroll 200 participants.

Study design
This is an interventional study that will randomly assign 200 participants to receive either empagliflozin or a placebo.
What's involved
You would take empagliflozin 10 mg or a placebo daily for 12 months. Baseline testing will be completed before starting the medication.
Compensation
Not stated in the trial record.
Follow-up
Your kidney health and any side effects will be measured at 12 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06625073

Randomized Trial of SGLT2i in Heart Transplant Recipients

Recruiting
PHASE4Ages 18+InterventionalTreatment
VA Office of Research and Development
~200 participants
Updated 2026-01-22 on ClinicalTrials.gov
What's tested:EmpagliflozinPlacebo

At a glance

Recruiting sites
1 of 6 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Urinary albumin-to-creatinine ratio (UACR)
Measured over 12 months
+1 more outcome measured
Heart Transplant
Cardiovascular Disease
Kidney Disease

NCT06625073

Where you'd take part

This study runs at 6 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Hunter Holmes McGuire VA Medical Center, Richmond, VA

    Richmond, Virginiastudy coordinator listed

    Not yet recruiting

  • Michael E. DeBakey VA Medical Center, Houston, TX

    Houston, Texasstudy coordinator listed

    Not yet recruiting

  • Tennessee Valley Healthcare System Nashville Campus, Nashville, TN

    Nashville, Tennesseestudy coordinator listed

    Not yet recruiting

  • VA Palo Alto Health Care System, Palo Alto, CA

    Palo Alto, Californiastudy coordinator listed

    Not yet recruiting

  • VA Salt Lake City Health Care System, Salt Lake City, UT

    Salt Lake City, Utahstudy coordinator listed

    Recruiting

  • William S. Middleton Memorial Veterans Hospital, Madison, WI

    Madison, Wisconsinstudy coordinator listed

    Not yet recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Josef Stehlik, MD MPH · PRINCIPAL_INVESTIGATOR · VA Salt Lake City Health Care System, Salt Lake City, UT

Opens a ready-to-send draft in your own email app — review before sending.

  • Urinary albumin-to-creatinine ratio (UACR)12 months

    UACR difference (mg/g) in subjects in active arm vs control arm

  • Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]12 months

    Adverse and serious adverse events difference in active arm vs control arm