Skip to content

A Study on the Effect of Recombinant Human Brain Natriuretic Peptide (rh-BNP) on Renal Function in Patients with Type 1 Cardiorenal Syndrome Based on the Venous Engorgement Ultrasound Grading System (VExUS)

A Study on the Effect of Recombinant Human Brain Natriuretic Peptide (rh-BNP) on Renal Function in Patients with Type 1 Cardiorenal Syndrome Based on the Venous Engorgement Ultrasound Grading System (VExUS)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105942
Enrollment
Unknown
Registered
2025-07-15
Start date
2025-07-20
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Type 1 Cardiorenal Syndrome

Interventions

Conventional diuretic group:Furosemide injection
Diuretic combined with rhBNP group:Furosemide injection+rh-BNP

Sponsors

Department of Critical Care Medicine, Tianjin First Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years; 2. Type 1 CRS (ultrasound indicating renal congestion or KDIGO AKI criteria); 3. MAP >= 65 mmHg; 4. Signs of congestion (edema, ascites, renal congestion, jugular vein distension, or pulmonary congestion); 5. NT-pro BNP: 450 ng/L; 50–75 years old >900 ng/L; >=75 years old >1800 ng/L; 6.After thorough communication, the patient agrees to participate in the study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Cardiogenic shock; 2. History of heart transplantation and/or ventricular assist device use; 3. Systolic blood pressure < 90 mmHg; 4. Baseline estimated glomerular filtration rate (eGFR) < 15 mL/min/1.73 m²; 5. Post-kidney transplantation; 6. Use of renal replacement therapy or ultrafiltration at any time prior to enrollment; 7. Expected exposure to nephrotoxic drugs (i.e., contrast agents) within 3 days; 8. Urinary tract obstruction; 9. End-stage malignant tumors; 10.Pregnant or breastfeeding women and patients with mental illness; 11. Patients who have difficulty participating in the study or undergoing follow-up, such as those who are non-compliant or have limited legal capacity; 12. Concurrent participation in other studies: Concurrent participation in other studies that may affect the results of this study or pose potential risks; 13.Allergy to the drugs involved in this study.

Design outcomes

Primary

MeasureTime frame
Left Ventricular Ejection Fraction;VExUS score;Improvement rate in renal function after 1 week of treatment;Renal congestion (based on ultrasound evaluation);

Secondary

MeasureTime frame
Improvement rate of dyspnea before treatment, 1 day after treatment, 3 days after treatment, 5 days after treatment, and 7 days after treatment;30-day readmission rate;Ratio of invasive mechanical ventilation within 30 days;Renal replacement therapy rate within 30 days;Number of days receiving intravenous diuretic therapy;Mitral Annular Plane Systolic Excursion;Left ventricular cardiac function index;Diameter of the inferior vena cava;

Countries

China

Contacts

Public ContactHongmei Gao

Department of Critical Care Medicine, Tianjin First Center Hospital

ghm182@163.com+86 130 7225 6661

Outcome results

None listed

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