About this trial
Zinc homeostasis could play a role in advanced chronic liver disease (cACLD) and its supplementation has been linked with improvement in liver function, decrease of hepatic complications and reduction in hepatocellular carcinoma (HCC) incidence. cACLD encompasses a heterogeneous group of patients with a variable risk of clinically significant portal hypertension (CSPH) and clinical events. The ANTICIPATE model is a validated model for stratifying these risks. Our aim is to demonstrate that the administration of zinc can reduce the rate and risk of presenting clinical events (first decompensation, HCC, death and liver transplantation). This study protocol describes an ongoing phase III, national, multicentre, randomized, double-blind clinical trial that will enroll 300 patients to receive either the trial treatment (zinc acexamate) or placebo. An inclusion period of 42 months is planned, with a minimal duration of follow up of 2 years. Our principal hypothesis is that zinc could modify the natural history of cACLD patients, with an overall improvement in prognosis
Eligibility criteria
Qualifiers
Patients of both sexes with diagnosed compensated advanced chronic liver disease (cACLD) determined by hepatic stiffness on transient elastography >15 kPa.
Age between 18 and 80 years, inclusive.
Absence of prior or current decompensation.
For women of childbearing age, a possible pregnancy will be ruled out by a pregnancy test prior to the start of the study. Following the test, the woman must use an effective contraceptive method during sexual intercourse (see Appendix I) in the days leading up to the start of treatment, and continue to use it throughout the treatment period, as well as for several days after its completion.
Disqualifiers
History or current presence of hepatocellular carcinoma.
Concomitant systemic disease with a short-term poor prognosis.
Pregnancy, breastfeeding, or refusal to use contraceptive measures during participation in the study.
Patients with compensated advanced chronic liver disease (cACLD) due to hepatitis B virus (HBV) under antiviral treatment, and those with cACLD due to hepatitis C virus (HCV) cured with antiviral treatment.
Trial design
Treatments tested in this trial
- Zinc Acexamate
Treatment groups
Sponsors and collaborators
Hospital Universitari Vall d'Hebron Research Institute
Lead sponsor
Hospital General Universitario Gregorio Marañon
Collaborator
Hospital Vall d'Hebron
Collaborator
Puerta de Hierro University Hospital
Collaborator
Hospital Clinic of Barcelona
Collaborator
Hospital Universitario Central de Asturias
Collaborator
Complejo Hospitalario de Toledo
Collaborator
Germans Trias i Pujol Hospital
Collaborator
Hospital Universitario Marqués de Valdecilla
Collaborator
Hospital Miguel Servet
Collaborator
Parc Taulí Hospital Universitari
Collaborator
Hospital de la Santa creu i Sant Pau - Barcelona
Collaborator
Hospital Universitari de Bellvitge
Collaborator
Hospital del Mar
Collaborator
University Hospital of Girona Dr. Josep Trueta
Collaborator