Zinc Supplementation to Improve Prognosis in Patients With Compensated Advanced Chronic Liver Disease.

Last updated: June 3, 2024
Sponsor: Hospital Universitari Vall d'Hebron Research Institute
Overall Status: Active - Recruiting

Phase

3

Condition

Diabetes And Hypertension

Liver Disorders

Carcinoma

Treatment

Zinc Acexamate

Clinical Study ID

NCT06434753
IC/LV/ACZ/PCHC
  • Ages 18-80
  • All Genders

Study Summary

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

Inclusion

Inclusion Criteria:

  • 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 pregnancytest prior to the start of the study. Following the test, the woman must use aneffective contraceptive method during sexual intercourse (see Appendix I) in thedays leading up to the start of treatment, and continue to use it throughout thetreatment period, as well as for several days after its completion.

  • Signing of informed consent.

Exclusion

Exclusion Criteria:

  • History or current presence of hepatocellular carcinoma.

  • Concomitant systemic disease with a short-term poor prognosis.

  • Pregnancy, breastfeeding, or refusal to use contraceptive measures duringparticipation in the study.

  • Patients with compensated advanced chronic liver disease (cACLD) due to hepatitis Bvirus (HBV) under antiviral treatment, and those with cACLD due to hepatitis C virus (HCV) cured with antiviral treatment.

Study Design

Total Participants: 300
Treatment Group(s): 1
Primary Treatment: Zinc Acexamate
Phase: 3
Study Start date:
October 02, 2022
Estimated Completion Date:
March 02, 2026

Connect with a study center

  • Hospital Universitari Vall d'Hebron

    Barcelona, 08035
    Spain

    Active - Recruiting

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