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Clostridium butyricum live tablets prevents hepatic encephalopathy after transjugular intrahepatic portosystemic shunt in portal hypertension: a randomized controlled study

Clostridium butyricum live tablets prevents hepatic encephalopathy after transjugular intrahepatic portosystemic shunt in portal hypertension: a randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070406
Enrollment
Unknown
Registered
2023-04-11
Start date
2023-04-15
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

hepatic encephalopathy (HE), portal hypertension

Interventions

Clostridium butyricum group:Clostridium butyricum 2 tablets/time 3 times/day
Lactulose 15ml/time, 3 times/day
Lactulose group:Lactulose 15ml/time, 3 times/day

Sponsors

Beijing Youan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years, no gender limit. 2. Patients treated with TIPS for portal hypertension (esophageal fundus variceal bleeding and/or recurrent chest/ascites) with or without cirrhosis. 3. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Previous episodes of hepatic encephalopathy. 2. Mental disorders, cognitive disorders, do not cooperate with the examination. 3. Unable or unwilling to retain stool specimens. 4. Patients with liver cancer and other malignant tumors. 5. Infected people who cannot be controlled. 6. Patients who underwent gastrointestinal surgery 3 months before enrollment. 7. Patients with other digestive tract diseases that may affect the intestinal microecology (such as ulcerative colitis, Crohn's disease, etc.). 8. TIPS or shunt surgery has been performed. 9. TIPS patients with shunt loss after surgery. 10. Pregnant patients.

Design outcomes

Primary

MeasureTime frame
Incidence of hepatic encephalopathy;

Secondary

MeasureTime frame
Time of occurrence of hepatic encephalopathy;Adverse reaction rate;Transplant free survival;Gut microbiota;Metabolomics;Laboratory outcome;Imaging results;

Countries

China

Contacts

Public ContactLi Jianjun

Beijing Youan Hospital,Capital Medical University

ljjir@163.com+86 138 1150 8978

Outcome results

None listed

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