About this trial
This is a retrospective-prospective registry cohort study. Patients with advanced chronic liver disease (ACLD) will be prospectively invited to this study. The study follow-up duration will be 10 years. The primary outcome is incident hepatic events and liver-related mortality. Participants will undergo annual transient elastography examination.
Eligibility criteria
Qualifiers
Aged 18 or above
LSM > 10kPa or
Clinical cirrhosis, suggested by 1. ultrasonography of the hepatobiliary system shows features of cirrhosis (e.g. shrunken and nodular liver) and portal hypertension (e.g. dilated portal vein, portal-systemic collaterals or varices, splenomegaly, ascites). 2. Oesophagogastroduodenoscopy (OGD) shows presence of oesophageal varices (OV) and/or gastric varices (GV) and/or portal hypertensive gastropathy.
Disqualifiers
Current or past history of hepatocellular carcinoma (HCC)
History of liver transplantation
Asplenism or history of splenectomy
Serious medical illness with limited life expectancy of less than 6 months
Trial design
Treatments tested in this trial
- Transient elastography