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Efficacy and safety of finelidone in patients with coronary heart disease and early renal disease combined with microalbuminuria

Efficacy and safety of finelidone in patients with coronary heart disease and early renal disease combined with microalbuminuria

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098674
Enrollment
Unknown
Registered
2025-03-12
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

coronary heart disease

Interventions

Experimental group:In addition to standard treatment for coronary heart disease, finelidone was given: 20mg orally once daily for 16 weeks.
Control group:standard treatment for coronary heart disease, including antiplatelet drugs and statins

Sponsors

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age > = 18 years old and 50% of major coronary arteries. 3eGFR>=60 mL/min/1.73 m²(CKD-EPI). 4. UACR>=30 mg/g and < 300 mg/g. 5. Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Suffering from dilated cardiomyopathy, chemotherapy-induced cardiomyopathy, hereditary hypertrophic cardiomyopathy, and infiltrative cardiomyopathy. 2. History of viral myocarditis and perinatal cardiomyopathy; Has a history of moderate or higher valvular disease. 3. At the same time, take RASi and Chinese patent medicines with proteinuria-lowering effect (Tripterygium wilfordii, Huang Kui, Bailing, Jin Shuibao, etc.). 4. Combined with diabetes mellitus (T1D, T2D, or HbA1c>=6.5%), hypertension, renal artery stenosis. 5. Suffering from rheumatic system diseases (currently using glucocorticoids or anti-rheumatic drugs). 6. Patients with malignant tumors. 7. History of drug or alcohol abuse in the past 12 months. 8. Vulnerable groups, including people with mental illness, cognitive impairment, critically ill patients, female subjects who are pregnant, lactating or have a positive pregnancy test, etc. 9. Other conditions that the investigator considers unsuitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Decrease in UACR from baseline at 16 weeks;

Secondary

MeasureTime frame
The magnitude of changes in eGFR, an indicator of renal function;Cardio-renal complex endpoints: renal failure, nephro-related death, cardiovascular death, hospitalization for heart failure;

Countries

China

Contacts

Public ContactZhang Wenbin

No. 3 Qingchun East Road, Hangzhou City, Zhejiang Province

3313011@zju.edu.cn+86 137 7757 2567

Outcome results

None listed

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