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Clinical Trials in the Netherlands / NCT05321706
Active, not recruiting Phase 3

DAPAgliflozin for Renal Protection in Heart Transplant Recipients

NCT05321706 · tracked via the Priya Life Science Netherlands tracker
Phase
Phase 3
Started
2022-06-08
Last updated
2026-07-01

Condition(s) studied

Heart Transplant FailureKidney Failure

Investigational drug(s) / intervention(s)

Dapagliflozin 10 mg →Placebo

Dapagliflozin 10 mg: Participants will be randomized in a 1:1 fashion to receive 10 mg of oral dapagliflozin

Placebo: Participants will be randomized in a 1:1 fashion to receive a matching placebo once daily for one year.

Study summary

Kidney failure is common in heart transplant recipients and is a major cause of morbidity and mortality. Sodium-glucose transporter 2 (SGLT2) inhibitors were developed as antidiabetics but were subsequently shown to reduce the incidence of adverse cardiovascular outcomes and protect renal function in non-diabetics as well as diabetics. However, SGLT2 inhibitors have not been tested in clinical trials in heart transplant recipients. The DAPARHT trial is designed to assess the effect of the SGLT2 inhibitor dapagliflozin to prevent deteriorating renal function in heart transplant recipients. Secondary objectives are to assess the impact of treatment on i) weight, ii) glucose homeostasis, iii) proteinuria, iv) the number of rejections, and (v) safety and tolerability. As exploratory outcomes, the investigators will assess the effect of treatment on renal outcomes, clinical events (death, myocardial infarction, cerebral stroke, cancer, and end-stage renal disease), cardiac function, quality of life, and new-onset diabetes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Heart transplant recipient ≥ 1 year after heart transplant. 2. Age ≥ 18 years Exclusion Criteria: 1. Contraindications to study medication. 2. Estimated GFR \< 25 ml/min/m2 3. Type I diabetes 4. Severe liver failure (Child-Pugh's score C) 5. Life expectancy reduced to \< 2 years as judged by the investigator 6. Unresolved malignant disease 7. Failure to obtain written informed consent 8. SGL2 inhibitor treatment over the last month 9. Pregnancy 10. Breast-feeding 11. Woman of child-bearing potential who is not willing to use a highly effective method of birth control

Primary outcome measure(s)

Trial sites (6)

FacilityCityRegionStatus
University Medical Center Groningen Groningen Netherlands
Erasmus Medical Center Rotterdam Netherlands
University Medical Center Utrecht Utrecht Netherlands
Oslo University Hospital, Rikshospitalet Oslo Oslo
Skane University Hospital Lund Sweden
Karolinska University Hospital Stockholm Sweden

More Oslo University Hospital trials in the Netherlands

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05321706 on ClinicalTrials.gov ↗ ← All trials in the Netherlands