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Finerenone for Cardiorenal Protection in Diabetic CKD: Impact on Renal Function Decline and Heart Failure

C

College of Physicians and Surgeons Pakistan

Status

Not yet enrolling

Conditions

Diabetic Kidney Disease (DKD)
Heart Failure

Treatments

Drug: Finerenone

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

To assess the effect of Finerinone on slowing renal function decline and improving cardiovascular outcomes, particularly heart failure risk, in patients with diabetic CKD.

Enrollment

120 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults aged ≥18 years.
  • Diagnosed cases of type 2 diabetes mellitus.
  • Chronic kidney disease with eGFR 25-90 mL/min/1.73m² and/or UACR ≥30 mg/g.
  • On stable ACE inhibitor or ARB therapy for at least 4 weeks.
  • Serum potassium ≤4.8 mmol/L.
  • Provided written informed consent.

Exclusion criteria

  • Symptomatic heart failure (NYHA class II-IV).
  • eGFR <25 mL/min/1.73m² or on maintenance dialysis.
  • Known non-diabetic kidney disease.
  • Recent major cardiovascular event (within 30 days).
  • Serum potassium >4.8 mmol/L or history of severe hyperkalaemia.
  • Contraindication or hypersensitivity to finerenone.
  • Pregnancy or lactation.
  • Any condition limiting compliance or follow-up.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

120 participants in 1 patient group

Finerenone Group
Experimental group
Description:
Finerenone Drug
Treatment:
Drug: Finerenone

Trial documents
1

Trial contacts and locations

0

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Central trial contact

Muhammad Awais Danish, FCPS (Internal Medicine)

Data sourced from clinicaltrials.gov

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