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NCT06449339
Non-selective Beta-blocker in Compensated Advanced Chronic Liver Disease
Conditions: Portal Hypertension, Hepatic Decompensation, Advanced Chronic Liver Disease
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE4
Enrollment: 474
Sponsor: Chinese University of Hong Kong
Location: Prince of Wales Hospital, The Chinese University of Hong Kong Hong Kong
Summary
The goal of this randomised controlled trial is to evaluate the effect of carvedilol (a non-selective beta-blocker) in patients with compensated advanced chronic liver disease under clinically significant portal hypertension or the grey zone of Baveno VII criteria.
The main question it aims to answer is:
Does carvedilol reduce hepatic decompensation and mortality in these patients despite the absence of varices needing treatment.
Researchers will compare carvedilol to no carvedilol to see if carvedilol can prevent hepatic decompensation and mortality.
Participants will either take carvedilol or not taking carvedilol for 5 years with regular clinic visit for checkups and investigations, including blood tests, ultrasonography of the liver, upper gastrointestinal endoscopy, transient elastography.
Eligibility Criteria
Inclusion Criteria:
* Aged 18 years of above
* Established diagnosis of chronic liver disease(s) of the following etiologies
* Alcohol-related liver disease (ARLD)
* Chronic hepatitis B (CHB)
* Chronic hepatitis C (CHC)
* Metabolic dysfunction-associated steatotic liver disease (MASLD) § Non-obese (BMI \
Source: ClinicalTrials.gov (NCT06449339). StuddyBuddy aggregates publicly available trial information.