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Clinical study of berberine in the treatment of sepsis with acute gastrointestinal injury

Clinical study of berberine in the treatment of sepsis with acute gastrointestinal injury

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082935
Enrollment
Unknown
Registered
2024-04-11
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Sepsis

Interventions

intervention group with Berberine:Berberine and compound vitamin B tablets were crushed into powder, dissolved in water, and fed nasally with a 50ml syringe 3 times a day for 7 days or patients were t
Control group:Compound vitamin B (similar in appearance to berberine) 2 tablets, administration route and method were consistent with the treatment group

Sponsors

General Hospital of Southern Theatre Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Hospitalized patients with sepsis and acute gastrointestinal injury, older than 18 years and younger than 80 years.

Exclusion criteria

Exclusion criteria: Acute central nervous system diseases (stroke, traumatic brain injury); Severe abdominal trauma; Acute myocardial infarction, severe arrhythmia, heart failure and shock (IABP), cardiopulmonary resuscitation; Primary neuromuscular disease; Drug, alcohol, opioid or amphetamine-type drug dependence, mental disorders; Pregnant women; Advanced malignant tumor or dysphoria, end-stage chronic disease; Patients expected to die within 24 hours in ICU; Past berberine allergy.

Design outcomes

Primary

MeasureTime frame
Classification of acute gastrointestinal injury;D-lactic acid;

Secondary

MeasureTime frame
lipolyaccharide;

Countries

China

Contacts

Public ContactLiu zhifeng

General Hospital of Southern Theatre Command

317542137@qq.com+86 137 1159 8120

Outcome results

None listed

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