About this trial
In patients with ESRD, up to 20% of patients suffer from HFrEF, leading to significant CV morbidity and mortality. Several drug classes that provide survival benefits for patients with HFrEF, including SGLT2i, lack data regarding their efficacy and safety in patients under chronic hemodialysis. As the primary target of SGLT2i is expressed mostly in the kidneys, the efficacy of SGLT2i in patients with ESRD may be limited. On the other hand, patients with ESRD are at higher risks of experiencing cardiovascular events and may still benefit from treatment. Several mechanistic studies have demonstrated direct actions of SGLT2i on the myocardium, thus it is possible that the benefits of SGLT2i on heart failure are independent of their glycosuric actions and may still be present in anuric subjects. Furthermore, pharmacokinetics and pharmacodynamics studies on empagliflozin demonstrated that peak plasma levels of empagliflozin in subjects with renal failure/ESRD were similar to those in subjects with normal renal function. The use of empagliflozin in patients with ESRD seemed safe in terms of pharmacokinetics and pharmacodynamics, yet its efficacy remains to be explored.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age ≥20 years old
ESRD under chronic, maintenance hemodialysis with stable dry weight for the past 6 months
Documented left ventricular ejection fraction <50% by any imaging modality within 1 month of screening
Disqualifiers
Age <20 years old
Ongoing pregnancy
NYHA class IV heart failure
Any hospitalization for heart failure within the past month
Trial design
Parallel
Treatments tested in this trial
Empagliflozin 25 MG
DrugThe medication will be packed in a customized sealed jar and labeled on the exterior of the jar.
Placebo
DrugThe placebo tablet is manufactured by Prince Pharmaceutical Co., Ltd, a leading manufacturer of nutritional supplements with certifications including cGMP, GMP, ISO, and HACCP. The Prince Pharmaceutical also provides Original Equipment Manufacturing (OEM)/Original Design Manufacturing (ODM) services for a wide array of tablet shapes, and post-processing techniques such as film coating and sugar coating.
Treatment groups
Trial outcomes
Primary outcomes
Left ventricular mass
As assessed by cardiac magnetic resonance imaging, performed on non-dialysis day
Secondary outcomes
Left ventricular mass index
As assessed by cardiac magnetic resonance imaging, performed on non-dialysis day
LV end-systolic volume index
As assessed by cardiac magnetic resonance imaging, performed on non-dialysis day
LV end-diastolic volume index
As assessed by cardiac magnetic resonance imaging, performed on non-dialysis day
LA volume index
As assessed by cardiac magnetic resonance imaging, performed on non-dialysis day
Sponsors and contacts
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National Taiwan University Hospital
Lead sponsor
Shin Kong Wu Ho-Su Memorial Hospital
Collaborator