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The Efficacy of Xuebijing Injection on Sepsis: A multicenter, blind, randomized placebo-controlled clinical trial

The Efficacy of Xuebijing Injection on Adult Patients with Sepsis: A multicenter, blind, randomized placebo-controlled clinical trial.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17012713
Enrollment
Unknown
Registered
2017-03-28
Start date
2017-10-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Sepsis

Interventions

Experimental:100ml Xuebijing Injection will be dissolved in 100 mL of normal saline every 12 hours for 5 days in blind fashion.
Placebo-controlled group:normal saline 200 ml every 12 hours for 5 days

Sponsors

ZhongDa Hospital, Affiliated to Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Sepsis-3 criteria from Society of Critical Care Medicine (SCCM) /European Society of Intensive Care Medicine (ESICM); 2. Aged 18 to 75 years; 3. SOFA 2 to 13; 4. obtain informed consent.

Exclusion criteria

Exclusion criteria: 1. 48 hours after diagnosis of sepsis; 2. Pregnancy or lactating; 3. Severe Primary disease such as uncontrolled and metastasis malignancy, hematopathy, HIV; 4. Severe, preexisting, parenchymal liver dysfunction or kidney dysfunction with SOFA=3; 5. Previous immunodepressant within 6 months before study entry or Receipt of a solid-organ or bone marrow transplant; 6. Participation in an investigational clinical trial within 30 days.

Design outcomes

Primary

MeasureTime frame
All-Cause Mortality;

Secondary

MeasureTime frame
Mortality in ICU;SOFA score;APACHE II;Duration of mechanical ventilation;ICU stay;

Countries

China

Contacts

Public ContactHaiBo Qiu

ZhongDa Hospital, Affiliated to Southeast University

haiboq2000@163.com+86 025 83262551

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 20, 2026