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Empagliflozin in ESKD - A Feasibility Study


Description

The aim of this study is to learn about the safety of empagliflozin in dialysis patients as a preparation for a future large clinical trial. Empagliflozin has been approved by the Food and Drug Administration for the treatment of either type 2 diabetes, heart failure, or chronic kidney disease among patients not on dialysis. The use of empagliflozin has not been studied or approved among patients on dialysis for kidney failure because empagliflozin acts on the kidneys. However, recent experimental studies have indicated that empagliflozin may provide direct heart benefits. Some dialysis patients have substantial residual kidney function, which may be protected by empagliflozin. Participants will be given empagliflozin for three (3) months on top of the standard of care (usual medical care for participants' condition) and will be followed up until one (1) month after the last dose. The investigators will collect information about participants' general health, obtain blood, urine, and i

Trial Eligibility

Inclusion Criteria: 1. age ≥18 years; 2. diagnosis of end-stage kidney disease requiring dialysis, and 3. ability to provide informed consent. Exclusion Criteria: 1. systolic blood pressure \<100 mm Hg (pre-dialysis for HD patients) 2. two or more episodes of urinary tract infection within the last 12 months 3. history of urinary retention or urinary tract obstruction 4. liver cirrhosis 5. advanced heart failure requiring heart assist device or inotropic support 6. heart or liver transplant recipient 7. major surgery performed within the last 3 months ("major" per the investigator's assessment) 8. major surgery scheduled within 3 months after screening ("major" per the investigator's assessment) 9. active cancer 10. pregnant or lactating women 11. known allergy or hypersensitivity to any SGLT2 inhibitors 12. history of ketoacidosis during the last 12 months 13. any other medical condition considered unappropriated by their nephrologists or a study physician (i.e., cachexia, short life expectancy, or uncontrolled personality/phycological disorder).

Study Info

Organization

University of Mississippi Medical Center


Primary Outcome

Proportion of eligible patients out of screened patients


Outcome Timeframe During the screening process

NCTID NCT05687058

Phases PHASE1,PHASE2

Primary Purpose TREATMENT

Start Date 2023-11-01

Completion Date 2025-04-30

Enrollment Target 24

Interventions

DRUG Empagliflozin 25 mg thrice-weekly post-hemodialysis dosing

DRUG Empagliflozin 10 mg daily dosing

Locations Recruiting

University of Mississippi Medical Center

United States, Mississippi, Jackson


Jackson Medicall Mall Dialysis Clinic

United States, Mississippi, Jackson


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