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Assessing the Cardiorenal Protective Effects of Finerenone in Combination with SGLT2 Inhibitors in Patients with Heart Failure

Assessing the Cardiorenal Protective Effects of Finerenone in Combination with SGLT2 Inhibitors in Patients with Heart Failure

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500115851
Enrollment
Unknown
Registered
2025-12-31
Start date
2025-12-31
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

heart failure

Interventions

Combination therapy group vs monotherapy group:NA

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years old; 2. Meets the diagnostic criteria for heart failure, with unlimited ejection fraction (including HFrEF, HFmrEF, HFpEF); 3. During the study period, one of the following prescriptions was prescribed for the first time: Combination therapy group: Simultaneously or within 30 days, non nifedipine and any SGLT2 inhibitors (such as dapagliflozin, empagliflozin, canagliflozin, etc.) were started and continued for at least 90 days. Monotherapy group: started using any SGLT2i and did not use any MRA (including non nalide, spironolactone, and eplerenone) for at least 6 months after starting medication, and continued medication for at least 90 days; 4. The medical records are complete, with at least baseline and one or more follow-up laboratory and cardiac ultrasound data.

Exclusion criteria

Exclusion criteria: 1. Previous renal replacement therapy (dialysis or kidney transplantation); 2. Baseline blood potassium>5.0 mmol/L; 3. Baseline estimated glomerular filtration rate (eGFR)<25 mL/min/1.73 m ²; 4. Key baseline variables (such as LVEF, NT proBNP, medication start time) are missing or logically contradictory and cannot be corrected; 5. During the follow-up period, there were no clinical records (outpatient, inpatient, laboratory, prescription), making it impossible to determine the primary endpoint status; 6. Simultaneously using other mineralocorticoid receptor antagonists (such as spironolactone, eplerenone) or multiple SGLT2 inhibitors violates the definition of exposure.

Design outcomes

Secondary

MeasureTime frame
Incidence rate of security incidents;Clinical outcome event incidence rate;Comprehensive improvement of cardiac function;Changes in Kidney and Metabolic Indicators;Imaging and functional indicators;

Primary

MeasureTime frame
Cardiac function evaluation;

Countries

China

Contacts

Public ContactRong Jiang

Shanghai General Hospital

listening39@163.com+86 21 63240090

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026