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Pharmacokinetics and Pharmacodynamics of Finerenone in Peritoneal Dialysis Patients

Pharmacokinetics and Pharmacodynamics of Finerenone in Peritoneal Dialysis Patients

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112969
Enrollment
Unknown
Registered
2025-11-21
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Chronic Kidney Diseases

Interventions

the finerenone group:NA

Sponsors

Provincial Hospital Affiliated to Fuzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Stable patients who have been on continuous ambulatory peritoneal dialysis (CAPD) in the Department of Nephrology of our hospital for more than 3 months and attend for routine CAPD assessment. 2. Aged 18–80 years. 3. Concomitant treatment with an ARB or ACEI for > 3 months. 4. Use of neutral-pH dialysis solution and/or icodextrin-based dialysate.

Exclusion criteria

Exclusion criteria: 1. Hyperkalemia (K? > 5 mmol/L) 2. Anemia (Hb < 9.0 g/dL) 3. NYHA Class III or IV heart failure 4. Use of acidic-pH dialysis fluid 5. Previous hemodialysis or kidney transplantation within the past 3 years, pregnancy or suspected pregnancy 6. Hepatic impairment, cholestasis, or biliary cirrhosis 7. Peritonitis or any severe systemic infection 8. Conditions that may interfere with follow-up, e.g., malignancy, drug or alcohol abuse 9. Severe psychiatric disorder

Design outcomes

Primary

MeasureTime frame
plasma-Finerenone;

Secondary

MeasureTime frame
urine-Finerenone;peritoneal dialysis fluid-Finerenone;

Countries

China

Contacts

Public ContactLin Miao

Provincial Hospital Affiliated to Fuzhou University

miul@163.com+86 135 0699 3517

Outcome results

None listed

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