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Evaluation of the Efficacy and Safety of Recombinant Human Brain Natriuretic Peptide in Real-World Treatment of Sepsis Complicated with Cardiac Dysfunction

Evaluation of the Efficacy and Safety of Recombinant Human Brain Natriuretic Peptide in Real-World Treatment of Sepsis Complicated with Cardiac Dysfunction

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124156
Enrollment
Unknown
Registered
2026-05-08
Start date
2026-05-08
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

sepsis with concomitant cardiac dysfunction

Interventions

recombinant human brain natriuretic peptide group:None

Sponsors

The Second Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Age 18–85 years; 2.Meeting the Sepsis-3 diagnostic criteria [defined as an increase of 2 points or more in the Sequential Organ Failure Assessment (SOFA) score from baseline in the context of infection]; 3.Presence of cardiac dysfunction during the course of sepsis treatment, regardless of a prior history of acute or chronic heart failure, with New York Heart Association (NYHA) functional class III or IV; 4.Signed informed consent obtained from the patient or their legally authorized representative (patients may be enrolled first in emergency situations and consent obtained thereafter);

Exclusion criteria

Exclusion criteria: 1.Known allergy to any component of recombinant human brain natriuretic peptide (rhBNP, brand name: Xinhuosu); 2.Presence of cardiogenic shock or systolic blood pressure < 90 mmHg (patients are eligible if the condition has improved and blood pressure has reached the target level after treatment, provided that the clinical course is clearly documented in the medical records); 3.Special populations, including those with significant valvular stenosis, hypertrophic or restrictive cardiomyopathy, constrictive pericarditis, or cardiac tamponade; 4.Suspected or confirmed low cardiac filling pressure; 5.End-stage renal disease requiring regular long-term dialysis; 6.Pregnant or breastfeeding women; 7.Expected survival < 24 hours (e.g., irreversible severe brain injury); 8.Refusal to participate in the study;

Design outcomes

Primary

MeasureTime frame
Assessment of Sequential Organ Failure;Changes in the Acute Physiology and Chronic Health Evaluation (APACHE II) score;

Secondary

MeasureTime frame
Degree of haemodynamic improvement;

Countries

China

Contacts

Public ContactGan Weini

The Second Affiliated Hospital of Guangxi Medical University

47059973@qq.com+86 771 3277106

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026