Overview

UDCA to Prevent Post-TIPS Hepatic Encephalopathy

Status:
NOT_YET_RECRUITING
Trial end date:
2027-12-31
Target enrollment:
Participant gender:
Summary
Hepatic encephalopathy (HE) commonly occurs after transjugular intrahepatic portosystemic shunt (TIPS). Ursodeoxycholic acid (UDCA) has been reported to alleviate neurodegenerative disease recently. This open-label multicenter randomized controlled trial tests whether adding UDCA (13-15 mg/kg/day) to standard lactulose prophylaxis reduces the incidence of overt HE (OHE; West Haven grade II-IV) after TIPS, compared with lactulose alone. The regimen starts within 72 hours before TIPS and continues for 3 months. The trial aims to evaluate the effect of UDCA in reducing the incidence of post-TIPS OHE.
Phase:
NA
Details
Lead Sponsor:
West China Hospital
Collaborators:
First Affiliated Hospital of Kunming Medical University
Qianjiang Central Hospital of Chongqing
The Second Affiliated Hospital of Chongqing Medical University
The Third People's Hospital of Kunming City
Treatments:
Lactulose
Ursodeoxycholic Acid