Chronic heart failure, chronic kidney disease Chronic heart failure, chronic kidney disease, peritoneal dialysis
Conditions
Interventions
The dapagliflozin group will receive 10 mg dapagliflozin orally once daily for 24 weeks
Sponsors
Yamamoto Suguru
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patients who provide written consent based on their own free will to participate in this study. 2) Patients who are 18 years of age or older 3) Patients who are undergoing peritoneal dialysis for the treatment of end-stage kidney disease for more than 3 months 4) Patients whose peritoneal dialysis regimen is stable for at least 4 weeks 5) Patients who are diagnosed with chronic heart failure and receiving standard treatment
Exclusion criteria
Exclusion criteria: 1) Patients who are participating in other clinical studies 2) Patients who are pregnant or breast feeding 3) Patients who have received SGLT2 inhibitors within 4 weeks 4) Patients who have received hemodialysis within 4 weeks 5) Patients who are treated for peritonitis within 4 weeks 6) Patients with a daily urine volume of less than 500 mL 7) Patients who have difficulty with infusion and drainage of peritoneal dialysis dialysate 8) Patients who are considering discontinuation of peritoneal dialysis within 8 weeks after enrollment. 9) Patients who have difficulty performing bioelectrical impedance analysis tests (pacemakers, and limb defects) 10) Patients who are allergic to dapagliflozin 11) Patients who are considered inappropriate to participate by investigators
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in extracellular water from baseline to week 24 | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) All-cause mortality events 2) First cardiovascular event (death due to cardiovascular disease, myocardial infarction, unstable angina, stroke and transient ischemic attack, pulmonary thromboembolism, and acute leg ischemia) 3) First event of hospitalization (excluding hospitalization for social reasons) 4) Duration of PD treatment 5) Change in body composition indices (body weight, BMI, ECW, ECW/height, ECW/body water) from baseline to week 24 6) Change in systolic and diastolic blood pressure from baseline to week 24 7) Change in Kt/V urea from baseline to week 24 8) Change in BNP from baseline to week 24 9) Change in echocardiographic parameters (LVDd, LVDs, LVEF, LVMI, LAD, E/A) from baseline to week 24 10) Change in D/P cr and D/D0 glu of dialysate at 4 hours by the frequently and short time peritoneal equilibration test (FAST PET)from baseline to week 24 11) Change in PD regimen (up, down, no change) from baseline to week 24 12) Weekly fluid removal (urine, PD, total) from baseline to week 24 | — |
Contacts
Public ContactSuguru Yamamoto
Niigata University Graduate School of Medical and Dental Sciences
Outcome results
None listed