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Discussion on the Mechanism of Novel Non-steroidal Mineralocorticoid Receptor Antagonists in the Treatment of Heart Failure with Preserved Ejection fraction

Discussion on the Mechanism of Novel Non-steroidal Mineralocorticoid Receptor Antagonists in the Treatment of Heart Failure with Preserved Ejection fraction

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126080
Enrollment
Unknown
Registered
2026-06-03
Start date
2026-06-03
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Heart Failure with Preserved Ejection Fraction,HFpEF

Interventions

Treatment group:Fineridone 20mg every day for 12 months.

Sponsors

The Second People's Hospital of Foshan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for HFpEF as defined in the Chinese Guidelines for the Diagnosis and Treatment of Heart Failure 2025: (1) Have the epidemiological and population characteristics of HFpEF patients; (2) Have symptoms and/or signs of heart failure (such as dyspnea, decreased exercise tolerance, edema, etc.); (3) LVEF >=50% on cardiac imaging (mainly TTE); (4) Have objective evidence of cardiac structural and/or functional abnormalities consistent with left ventricular diastolic dysfunction and/or elevated left ventricular filling pressure. 2. New York Heart Association (NYHA) functional class II-IV, with symptoms and signs of heart failure. 3. Elevated NT-proBNP (>450 pg/mL for age 900 pg/mL for age 50-75 years, >1800 pg/mL for age >75 years) or B-type natriuretic peptide (BNP) >100 pg/mL. 4. Echocardiographic evidence of cardiac structural changes (such as increased left atrial size or left ventricular mass). 5. Age >=18 years.

Exclusion criteria

Exclusion criteria: 1. Patients with severe liver and kidney and other important organ disorders; 2. Patients with contraindications to the treatment and evaluation methods of this study; 3. Patients with acute and chronic infectious diseases; 4. Patients with acute decompensated heart failure; 5. Acute coronary syndrome occurred one month before screening, and coronary revascularization (percutaneous coronary intervention or coronary artery bypass grafting) or valve repair/replacement was performed; 6. Patients using finerenone within 1 month; 7. Patients with poor compliance. 8. BMI>50 kg/m^2.

Design outcomes

Primary

MeasureTime frame
Peak time of myocardial segments (tpeak);Maximum ascending slope (Slopemax) of myocardial signal intensity;Peak signal intersity, SIpeak;

Secondary

MeasureTime frame
Left ventricular end diastolic diameter,LVEDD;Left ventricular ejection fraction ,LVEF;6-minute walking distance,6MWT;Minnesota Heart Failure Quality of Life Scale score,MHFQL;N-terminal pro-brain natriuretic peptide (NT-proBNP);Urinary microalbumin/urinary creatinine;Adverse event;

Countries

China

Contacts

Public ContactZhang Zhenhong

The Second People's Hospital of Foshan

26061704@qq.com+86 139 0284 1211

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026