RecruitingPhase 2NCT06929169

Cardiovascular Effects of SGLT2 Inhibitors in Hemodialysis Patients: A Phase 2 Randomized Study


Sponsor

Maximo Agustin Schiavone

Enrollment

80 participants

Start Date

May 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Patients with end-stage kidney disease (ESKD) on hemodialysis face an unacceptably high rate of cardiovascular complications, including heart failure, arrhythmias, and sudden cardiac death. Many of these outcomes are driven by diastolic dysfunction and cardiac fibrosis-conditions that are not adequately addressed by current therapies. SGLT2 inhibitors, originally developed for the treatment of type 2 diabetes, have demonstrated cardiovascular and renal protective effects across multiple patient populations, independent of glycemic control. This Phase 2, randomized, controlled clinical trial will evaluate the safety and efficacy of SGLT2 inhibitors in patients undergoing maintenance hemodialysis. A total of 80 participants will be randomized to receive either an SGLT2 inhibitor or standard care for 12 months. The primary objective is to determine whether SGLT2 inhibitors improve cardiac function, reduce myocardial fibrosis, and decrease the incidence of intradialytic hypotension. Secondary endpoints include cardiovascular events, hospitalization, and all-cause mortality. The study will also assess changes in key biomarkers and perform advanced cardiac imaging to evaluate structural and functional outcomes. This trial represents a novel and timely investigation into a class of medications with promising pleiotropic effects, potentially offering new therapeutic options for a high-risk, underserved population.


Eligibility

Min Age: 18 YearsMax Age: 70 Years

Plain Language Summary

Simplified for easier understanding

This Phase 2 study looks at whether a class of diabetes/heart medications called SGLT2 inhibitors can help protect the heart in people with end-stage kidney disease who are on dialysis. It uses heart MRI scans to measure changes in heart function. **You may be eligible if...** - You are between 18 and 70 years old - You have end-stage kidney disease (your kidneys no longer function adequately) - You have been on dialysis (hemodiafiltration) for at least 3 months - You are able to provide written consent **You may NOT be eligible if...** - You have type 1 diabetes - You have a history of diabetic ketoacidosis (a serious diabetes complication) - You have previously received a kidney transplant - You are allergic to or cannot tolerate SGLT2 inhibitor medications - You cannot have an MRI scan - You had a heart attack within the past 30 days - You are currently taking an SGLT2 inhibitor Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGiSGLT2

Participants randomized to the experimental arm will receive a once-daily dose of a sodium-glucose cotransporter 2 inhibitor (SGLT2i), administered orally, in addition to their standard hemodialysis care. The specific agent (e.g., dapagliflozin or empagliflozin) and dose will be selected based on safety data and clinical guidelines applicable to patients with end-stage renal disease (ESRD) on dialysis. The intervention will be maintained for 12 months. Dosing will be monitored by the research team to ensure tolerability and adherence. All patients in the experimental group will undergo comprehensive cardiovascular assessment, including serial cardiac MRI, echocardiography, and measurement of fibrosis-related biomarkers. This intervention differs from standard care by introducing a pharmacologic agent not routinely administered in the dialysis population, targeting cardiac remodeling, fibrosis, and intradialytic complications.


Locations(1)

Fresenius Medical Care - CEMIC Saavedra

Buenos Aires, Buenos Aires, Argentina

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NCT06929169


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