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Efficacy and safety of tauroursodeoxycholic acid in the treatment of liver cirrhosis: a double-blind randomised controlled trial

Efficacy of tauroursodeoxycholic acid in the treatment of liver cirrhosis: a double-blind randomised controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12001939
Enrollment
Unknown
Registered
2012-02-14
Start date
2009-06-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

liver cirrhosis

Interventions

TUDCA group:750mg/d, oral
UDCA group:750mg/d, oral

Sponsors

Department of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: cirrhosis based on the standard criteria revised at 2000 by the branch of infectious, parasitic diseases and hepatic association of Chinese medical association; age between 18 and 75 years; written informed consent.

Exclusion criteria

Exclusion criteria: Body mass index (BMI)>28kg/m2; serum total bilirubin concentration >=171umol/L; hepatic failure who need hepatic transplantation; malignancies; gallbladder disease; active gastrointestinal bleeding; hepatic encephalopathy; hepatorenal syndrome; intestinal infection; peptic ulcer; severe heart and renal dysfunction; severe endocrine, hematologic and neuropsychiatric diseases; pregnancy or lactation. Patients were also excluded if they had been treated with interferon, UDCA, colchicine, anti-virus or immunomodulatory drugs in the previous 3 months.

Design outcomes

Primary

MeasureTime frame
alanine aminotransferase;aspartate aminotransferase;alkaline phosphatase;gamma-glutamyltransferas;

Secondary

MeasureTime frame
serum markers of liver fibrosis;liver histologic stage;

Countries

China

Contacts

Public ContactXiaohua Hou
yejin8688@sina.com+86 27 85726057

Outcome results

None listed

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