About this trial
This study investigated the use of novel plasma and urinary biomarkers to predicte the development of hepatorenal syndrome in patients with advanced cirrhosis. The biomarkers investigated include plasma cystatin C, plasma NGAL, plasma NAG, plasma IL-18, plasma ADMA, plasma BTP, urinary KIM-1 and urinary LFABP. These biomarkers will be checked in advanced cirrhotic patients who have or have not developed hepatorenal syndrome and compared between the two groups. These biomarkers will also be correlated with the occurence of hepatorenal syndrome.
Eligibility criteria
Qualifiers
Patients with advanced cirrhosis (Child's B or C) referred for liver transplantation
Willing to give informed consent
Disqualifiers
Patients with co-existing renal diseases
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
The University of Hong Kong
Lead sponsor
The Hong Kong Society of Nephrology
Collaborator