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Efficacy and Safety of Xuebijing Injection in Preventing Acute Gastrointestinal Injury in Patients with Sepsis: A Randomized Controlled Trial

The efficacy and safety of Xuebijing Injection in treating acute gastrointestinal injury in patients with sepsis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122788
Enrollment
Unknown
Registered
2026-04-17
Start date
2022-03-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Sepsis

Interventions

Xuebijing group:100mL of Xuebijing Injection and 100mL of 0.9% sodium chloride Injection are diluted and administered intravenously twice a day for a course of 7 days
Control group:100mL of 0.9% sodium chloride injection (the same as the appearance placebo) was intravenously infused twice a day for a course of 7 days

Sponsors

Ningbo Zhenhai District Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old; 2. Meet the diagnostic criteria of sepsis 3.0; 3. No AGI occurred at the time of enrollment (AGI grade 0; 4. The estimated length of stay in the ICU is >=72 hours; 5. The patient or his/her legal representative signs a written informed.

Exclusion criteria

Exclusion criteria: 1. The primary infection site is located in the gastrointestinal tract. 2. There was a history of chronic gastrointestinal failure or major gastrointestinal surgery before enrollment; 3. Known to be allergic to the components of Xuebijing Injection; 4. Pregnancy or lactation period; 5. Severe underlying diseases such as advanced malignant tumors that may interfere with endpoint assessment; 6. Participate in other interventional clinical trials simultaneously; 7. Any level of AGI already existed at the time of enrollment.

Design outcomes

Primary

MeasureTime frame
The incidence of AGI (grade >= I);

Secondary

MeasureTime frame
The time until AGI occurs;28-day all-cause mortality rate;Length of stay in the ICU and total length of stay;SOFA score and APACHE II score;Duration of mechanical ventilation;inflammatory markers;Feeding tolerance indicators;

Countries

China

Contacts

Public ContactLi Fang

Ningbo Zhenhai District Hospital of Traditional Chinese Medicine

li_fang0@hotmail.com+86 176 1095 2232

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026