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Clinical study on hemodynamic evaluation of participants with septic shock using freeze-dried recombinant human brain natriuretic peptide

Clinical study on hemodynamic evaluation of participants with septic shock using freeze-dried recombinant human brain natriuretic peptide

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102842
Enrollment
Unknown
Registered
2025-05-20
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Patients with NYHA classification > II who require treatment with natriuretic peptide

Interventions

Observation group within natriuretic peptide treatment:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18; 2. Participants with NYHA classification > II who require treatment with natriuretic peptide; 3. Informed consent of the patients or their families and approval by the ethics committee.

Exclusion criteria

Exclusion criteria: 1. Maternal; 2. Participants with an expected survival time of less than 72 hours; 3. Participants 80 years of age (older participants have greater variation in physiological functioning, which may bias study results); 4. Irreversible heart disease (e.g., end-stage cardiomyopathy) existed prior to the disease; 5. Participants in whom hemodynamic, tests and ultrasound indices cannot be taken prior to the application of natriuretic peptide.

Design outcomes

Primary

MeasureTime frame
Blood pressure;Heart rate;Urine output;Mean arterial pressure(MAP);Central venous pressure (CVP);Central venous oxygen saturation;Arteriovenous carbon dioxide partial pressure difference;24h access;Type, dosage and duration of vasoactive drug use, etc.;Type, dosage and duration of cardiac drug use, etc.;Myocardial markers;Left Ventricular Ejection Fraction(LVEF);Stroke Volume(SV);Cardiac Output Index (CI);Left Ventricular Outflow Tract Velocity-Time Integral(LVOT-VTI);Tricuspid Annular Plane Systolic Excursion(TAPSE);Mitral Annular Systolic Excursion(MAPSE);Mitral Inflow E/A Ratio (E/A);E/e' Ratio;Inferior vena cava (IVC) long-axis and short-axis measurements and collapsibility index;Valve regurgitation conditions;Cardiac contraction (presence of abnormal segmental contractions);Ultrasound presentation of the lungs;ICU 28-day mortality rate;Duration of mechanical ventilation;Costs during ICU stay;Total hospitalisation costs;Sexes;Age;Primary disease;Antecedent history;Acute Physiology And Chronic Health Evaluation II (APACHE II);Sequential Organ Failure Assessment (SOFA);Intracranial blood flow;Renal and gastrointestinal perfusion (microcirculation improvement);The time required for stable blood pressure;Significant correction time for shock;Duration of shock;Occurrence and number of organs affected by MODS;Total difference in infusion volume (fluid balance) within 7 days after admission to the ICU;

Secondary

MeasureTime frame
Routine blood test;Liver function;Renal function;Coagulation;Arterial blood gases (pH, oxygen partial pressure, carbon dioxide partial pressure, lactate, oxygenation index);Mechanical ventilation parameters;Surveillance of site of infection and infectious agents (sputum culture, blood culture, bronchoalveolar lavage culture, NGS, PCR, etc.);ICU 14-day mortality rate;

Countries

China

Contacts

Public ContactYin Wanhong

West China Hospital of Sichuan University

179319164@qq.com+86 187 1530 9637

Outcome results

None listed

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