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Effects of recombinant human brain natriuretic peptide on IL-1 ß/IL-18 and ventricular remodeling in patients with acute heart failure

Effects of recombinant human brain natriuretic peptide on IL-1 ß/IL-18 and ventricular remodeling in patients with acute heart failure

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119018
Enrollment
Unknown
Registered
2026-02-13
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Acute attack of acute heart failure

Interventions

Receive standardized heart failure treatment and individualized medication therapy, excluding rhBNP.:None
Receive standardized heart failure treatment combined with rhBNP:None

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.The patient had symptoms and signs of emergency heart failure, and was diagnosed with acute heart failure (ESC 2021 diagnostic criteria), LVEF<40%; 2.The patients were aged from 18 to 80 years old and had no history of exacerbation of heart failure (excluding the interference of chronic remodeling); 3.Patients received standardized treatment (diuretics+vasodilators ± positive inotropic drugs). 4.Patients and their families signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients complicated with infection, tumor and autoimmune diseases (to avoid interference of inflammatory indicators); 2.The patient received IL-1 ß antagonist or immunosuppressive therapy within 3 months; 3.The patient is allergic to any component of recombinant human brain natriuretic peptide, accompanied by cardiogenic shock or systolic blood pressure2.0 times the upper limit of normal value) and renal dysfunction (egfr<60); 5.Patients with hematological diseases, mental diseases or systemic diseases; 6.Women during pregnancy or lactation; 7.Patients participating in clinical research of other drugs;

Design outcomes

Primary

MeasureTime frame
NT-proBNP;Type of heart failure;Difference in GSDMD changes from baseline between the two groups after 72 hours of treatment;

Secondary

MeasureTime frame
Rehospitalization time;Interleukin-6;Dyspnea;coronary heart disease;Interleukin-1 ß;weight;diabetes;Interleukin-18;edema;Tumor Necrosis Factor-alpha;height;New York Heart Association Classification;hypertension;Treatment plan;Cardiac ultrasound;Time of major adverse cardiovascular events;Long term medication;hs - CRP;Major Adverse Cardiovascular Events;

Countries

China

Contacts

Public ContactLijun Cao

Qilu Hospital of Shandong University

csq44@sina.com+86 531 5566 7788

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026