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Registry Study of Recombinant Human Natriuretic Peptide in Hospitalized Patients with Acute Heart Failure

Registry Study of Recombinant Human Natriuretic Peptide in Hospitalized Patients with Acute Heart Failure

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112782
Enrollment
Unknown
Registered
2025-11-19
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Acute Heart Failure

Interventions

rhBNP treatment group:NA

Sponsors

FUWAI Hospital, CAMS&PUMC
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years, regardless of gender. 2. Diagnosed with acute heart failure according to the National Heart Failure Guidelines 2023. 3. Patients scheduled to receive recombinant human natriuretic peptide treatment. 4. NT-proBNP >= 450 ng/L at screening. 5. Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Cardiogenic shock or persistent systolic blood pressure < 90 mmHg. 2. Diagnosed with severe valvular stenosis, hypertrophic cardiomyopathy, constrictive pericarditis, cardiac tamponade, or severe pulmonary disease. 3. Pregnancy or lactation. 4. Known or suspected allergy to the investigational drug or its components. 5. Participation in other clinical studies within the past month. 6. Any other condition deemed unsuitable for inclusion by the investigator.

Design outcomes

Primary

MeasureTime frame
Rate of dyspnea improvement at 24 hours ;Change from baseline in serum creatinine (SCr), estimated glomerular filtration rate (eGFR), serum potassium, and Cystatin C at 24h, 72h, and 30 days ;Length of hospital stay for the current acute heart failure episode;30-day and 90-day all-cause mortality + heart failure rehospitalization rate;0-day and 90-day cardiovascular mortality + heart failure rehospitalization rate;

Secondary

MeasureTime frame
dyspnea improvement;dyspnea improvement (assessed by the 7-point Likert scale) at other time points besides 24h of treatment (3h, 48h, 72h, 96h, 120h, 6 days, 7 days);Change from baseline in NT-proBNP levels at 24h, 48h, 72h, 96h, 120h, and 30 days after initiation of treatment;Change from baseline in 24-hour urine output during hospitalization;

Countries

China

Contacts

Public ContactJian Zhang and Yuhui Zhang

FUWAI Hospital, CAMS&PUMC

yuhuizhangjoy@163.com+86 159 0131 4243

Outcome results

None listed

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