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Clinical Trials in China / NCT07603024
Starting soon Not applicable

Effect of Shenfu Injection on the Vascular Waterfall Phenomenon in Patients With Septic Shock

NCT07603024 · tracked via the Priya Life Science China tracker
Sponsor
First Affiliated Hospital of Wannan Medical College
Phase
Not applicable
Started
2026-07-01
Last updated
2026-05-22

Condition(s) studied

Septic Shock

Investigational drug(s) / intervention(s)

Shenfu Injection

Shenfu Injection: All participants in the study will receive a single intravenous infusion of Shenfu Injection, a traditional Chinese medicine produced by China Resources Sanjiu Pharmaceutical Co., Ltd. The injection contains extracts of Ginseng Radix et Rhizoma and Aconiti Lateralis Radix Praeparata. Each dose consists of 100 mL Shenfu Injection, diluted in 250 mL normal saline, and administered through continuous intravenous infusion over 1 hour after initial hemodynamic stabilization according to Surviving Sepsis Campaign guidelines. Hemodynamic measurements will be performed before infusion (within 30 minutes) and at 3 hours after infusion. Variables include critical closure pressure (Pcc), mean systemic filling pressure (Pmsf), cardiac index, systemic vascular resistance, central venous oxygen saturation, arterial-venous CO₂ difference, and blood lactate concentration. No other investigational drugs, placebos, or control interventions are administered in this study.

Study summary

This prospective single-center clinical trial aims to evaluate the circulatory and microcirculatory effects of Shenfu Injection in patients with septic shock. The study focuses on the vascular waterfall phenomenon, which describes the relationship between arterial and venous pressures in the microcirculation.

Eligible participants with septic shock will receive an intravenous infusion of 100 mL Shenfu Injection (manufactured by China Resources Sanjiu Pharmaceutical Co., Ltd.). Hemodynamic and oxygen metabolism parameters will be measured before and 3 hours after treatment. The main goal is to determine whether Shenfu Injection influences the vascular waterfall difference, expressed as the gap between critical closure pressure and mean systemic filling pressure.

This study will also record changes in cardiac index, systemic vascular resistance, blood lactate, venous oxygen saturation, and norepinephrine requirement. Findings will provide preliminary clinical evidence about the role of Shenfu Injection in circulatory regulation during septic shock and help design future randomized controlled studies.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
nclusion Criteria Septic shock diagnosed according to Sepsis-3 criteria after adequate fluid resuscitation. Age ≥ 18 years. Within 24 hours of ICU admission. Receiving norepinephrine ≥ 0.10 µg/kg/min to maintain mean arterial pressure ≥ 65 mmHg. Hemodynamically stable without vasopressor dose adjustment for ≥ 30 minutes before baseline measurement. Endotracheal intubation with controlled mechanical ventilation under continuous sedation and analgesia. Presence of both arterial and central venous catheters with PiCCO monitoring capability. Written informed consent obtained from the patient or legally authorized representative. Exclusion Criteria Cardiogenic shock as primary diagnosis or cardiac index \< 2.2 L/min/m² after optimization. Severe pulmonary bullae, pneumothorax, or conditions precluding safe inspiratory hold maneuvers. Pregnancy or lactation. Expected ICU stay \< 48 hours or limitation of life-sustaining therapy. Known allergy or contraindication to Shenfu Injection or its ingredients (e.g., ginseng, aconitum).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College) Wuhu Anhui

More First Affiliated Hospital of Wannan Medical College trials in China

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07603024 on ClinicalTrials.gov ↗ ← All trials in China