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A Study on the Efficacy and Safety of Finerenone on Cardiac and Renal Function in Patients with Coronary Artery Disease and Diabetes

A Study on the Efficacy and Safety of Finerenone on Cardiac and Renal Function in Patients with Coronary Artery Disease and Diabetes

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124836
Enrollment
Unknown
Registered
2026-05-18
Start date
2026-05-18
Completion date
Unknown
Last updated
2026-05-25

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

Conditions

Coronary heart disease combined with diabetes

Interventions

The non-naliniotone group:Patients in the finerenone group were given finerenone in addition to conventional treatment (initial dose of 10mg, once daily, and subsequently adjusted to 20mg, once daily
Control group:The control group received drug treatment based on the conventional treatment plan by the clinical physicians: lowering blood sugar (metformin tablets, dapagliflozin tablets, insulin, et

Sponsors

Pharmacy Department of Su Bei People's Hospital, Jiangsu Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. In accordance with the "Diagnostic Criteria for Coronary Artery Atherosclerotic Heart Disease": any major coronary artery such as the left main trunk, left anterior descending branch, left circumflex branch, right coronary artery or its main branch is narrowed by >=50%; in accordance with the "Diagnosis Criteria for Type 2 Diabetes Mellitus in China 2010 Edition": fasting plasma glucose (FPG) >= 7.0 mmol/L, 2-hour blood glucose after oral glucose tolerance test >= 11.1 mmol/L; 2. Age >= 45 years old, gender not limited; 3.Serum potassium = 25 ml/min/1.73 m^2; 5.Total follow-up time is not less than 3 months. Overall, 20 mg, once daily)

Exclusion criteria

Exclusion criteria: 1.Patients with severe liver or kidney dysfunction, myocarditis, heart valve disease, cardiomyopathy, or malignant tumors; 2. Patients with infectious diseases, thyroid disorders, or mental illnesses; 3. Patients with incomplete clinical data; 4. Patients with hyperkalemia > 5.0 mmol/L; 5. Patients allergic to the drug nonalnidin.

Design outcomes

Primary

MeasureTime frame
Left ventricular ejection fraction;Urinary albumin to creatinine ratio;Creatinine;Serum potassium;urea;

Countries

China

Contacts

Public ContactLiu Jia

Pharmacy Department of Su Bei People's Hospital, Jiangsu Province

liujia85912@163.com+86 180 5106 0032

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026