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Clinical study on the efficacy of recombinant human brain natriuretic peptide combined with levosimendan in patients with heart failure and its influence on the levels of LVEF, NT-proBNP and myocardial injury markers

Clinical study on the efficacy of recombinant human brain natriuretic peptide combined with levosimendan in patients with heart failure and its influence on the levels of LVEF, NT-proBNP and myocardial injury markers

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122263
Enrollment
Unknown
Registered
2026-04-10
Start date
2026-04-10
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Heart failure

Interventions

experimental group:Combined use of Lusemendan based on the control group.
Control group,:On top of basic treatment, treat with recombinant human brain natriuretic peptide

Sponsors

Meizhou People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for heart failure and is a patient with acute chronic heart failure (AHF); 2. Age between 18 and 75 years; 3. New York Heart Association (NYHA) functional classification II-IV; 4. Patient or their family has signed the informed consent form and voluntarily participates in this study; 5. No other severe heart diseases or comorbidities, such as acute myocardial infarction, severe arrhythmias, etc.

Exclusion criteria

Exclusion criteria: 1. Severe liver or kidney dysfunction that may affect drug metabolism and excretion; 2. Allergy to recombinant human brain natriuretic peptide or levosimendan; 3. Recent (within 3 months) cardiac surgery or interventional treatment; 4. Severe neurological or psychiatric disorders affecting the evaluation of treatment efficacy; 5. Participation in other clinical trials that may affect the accuracy of this study's results.

Design outcomes

Primary

MeasureTime frame
left ventricular ejection fraction, LVEF ;N-terminal Pro-brain Natriuretic Peptide, NT-proBNP;

Secondary

MeasureTime frame
Quality of life;

Countries

China

Contacts

Public ContactLi Pu

Meizhou People's Hospital

735300500@qq.com+86 753 213 1026

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026