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Clinical Observation on the Effect of Recombinant Human Brain Natriuretic Peptide in Improving Cardiac Function in Patients with Heart Failure

An Observational Study on the Improvement of Mitochondrial Function and the Relief of Heart Failure by Recombinant Human Brain Natriuretic Peptide

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114718
Enrollment
Unknown
Registered
2025-12-17
Start date
2026-01-04
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Diagnosed as acute decompensated heart failure

Interventions

Standard Therapy Group:NA
Standard Therapy + rhBNP Group:NA

Sponsors

Xuanwu Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age 18 years or above, and gender not limited. 2. Clinically diagnosed as ADHF (NYHA cardiac function classification: grade III-IV); 3. Expected hospitalization duration >= 72 hours; 4. Systolic blood pressure >= 100 mmHg; 5. Sign the informed consent form;

Exclusion criteria

Exclusion criteria: 1. Patients who are allergic to any component of recombinant human brain natriuretic peptide; 2. Patients who were using ARNI before admission (and had been using it continuously prior to hospitalization); 3. Patients with untreated tumors; 4. Pregnant women, lactating women, or those planning to become pregnant within the next 3 months; 5. Patients with severe renal insufficiency requiring dialysis; 6. Patients with major organ dysfunction or failure; 7. Within 30 days prior to signing the informed consent form, one has participated in other clinical studies and received trial interventions (such as trial drugs or medical devices), or is still within the visit period of another clinical study. 8. The researchers believe that any other situation that might pose risks to the patients;

Design outcomes

Primary

MeasureTime frame
Change in NT-proBNP level;

Secondary

MeasureTime frame
30-day readmission rate for heart failure;

Countries

China

Contacts

Public ContactZhi Liu

Xuanwu Hospital, Capital Medical University

liuzhi7742@sina.com+86 10 83198382

Outcome results

None listed

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