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Effectiveness and safety of washed intestinal microbiota transplantation in the treatment of hepatitis B-related acute-on-chronic liver failure: A Dual-Center, Prospective, Open-Label Clinical Study

Effectiveness and safety of washed intestinal microbiota transplantation in the treatment of hepatitis B-related acute-on-chronic liver failure: A Dual-Center, Prospective, Open-Label Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088973
Enrollment
Unknown
Registered
2024-08-29
Start date
2024-09-16
Completion date
Unknown
Last updated
2024-09-02

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

Conditions

Hepatitis B-related acute-on-chronic liver failure

Interventions

Wash intestinal bacteria treatment group:Wash intestinal bacteria transplantation
Conventional treatment group:Conventional treatment

Sponsors

First Affiliated Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1: Patients who are willing to sign informed consent; 2: Patients aged 18-60 years; 3: Diagnosing patients with HBV-related acute-on-chronic liver failure, classified as type A or type B, and staged as early or intermediate.

Exclusion criteria

Exclusion criteria: 1: Combined with HIV infection, hepatitis A, C, D, E virus infection, drug liver disease, alcoholic liver disease, etc.; 2: Type C liver failure, late liver failure; 3: Patients with severe heart failure, chronic obstructive pulmonary disease, cerebrovascular accident, gastrointestinal bleeding, etc. 4: Combined with primary peritonitis; 5: Bacterial or fungal infection of lung, urinary system and blood. 6: Combine patients with liver cancer, lung cancer, lymphoma, etc. malignant tumors; 7: Patients who have been taking anticoagulants for a long time, patients with mental and immune diseases; 8: Pregnant women or lactating women; 9: Patients who take antibiotics orally or intravenously; 10: Patients with CD4+ cells less than 200×10^6/mL.

Design outcomes

Primary

MeasureTime frame
90-day survival rate;

Secondary

MeasureTime frame
The incidence of upper gastrointestinal bleeding, hepatic encephalopathy, and hepatorenal syndrome within 90 days;

Countries

China

Contacts

Public ContactJinshui Pan

First Affiliated Hospital of Fujian Medical University

363111396@qq.com+86 136 6608 3256

Outcome results

None listed

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