HUTCH: Chronic Hepatitis B Virus Infection in Zambia

Sponsor
University of Alabama at Birmingham (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03158818
Collaborator
Tropical Gastroenterology and Nutrition Group (Other), Centre for Infectious Disease Research in Zambia (Other)
326
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95.3
3.4

Study Details

Study Description

Brief Summary

Chronic hepatitis B virus infection is a common condition in Zambia. Among Zambian blood donors, up to 8% are chronically infected with HBV. Despite the burden, awareness of HBV is low in Zambia and the Ministry of Health is in early stages of development of guidelines for HBV screening, treatment, and prevention. The purpose of this clinical cohort study is to characterize the clinical features of chronic HBV infection at UTH and describe treatment and care outcomes. The investigators will enroll 500 adults and follow the cohort for up to 5 years to assess short and long-term viral, serologic, and liver outcomes such as cirrhosis and liver cancer.

Condition or Disease Intervention/Treatment Phase
  • Other: Standard of care

Detailed Description

Viral hepatitis is the #7 cause of death worldwide, yet it has been neglected when compared to other infectious diseases such as HIV/AIDS, tuberculosis, and malaria. Chronic viral hepatitis is caused by hepatitis C virus and hepatitis B virus and these infections are most common in low and middle-income countries, notably Asia and sub-Saharan Africa. In Zambia there are limited data, but from an HIV cohort, the investigators of this study described 10-12% prevalence of chronic HBV. To raise awareness of viral hepatitis in Zambia and to generate local data to guide policymakers, the investigators will recruit 500 adults with chronic HBV infection and follow the cohort in an observational cohort study. In the study patients would be managed according to standards of care and no experimental or investigational drugs would be used. The investigators will carefully describe patient clinical characteristics and among those who receive drug treatment, the investigators will describe the effectiveness of that treatment in reducing liver disease.

Study Design

Study Type:
Observational
Actual Enrollment :
326 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Chronic Hepatitis B Virus Infection in Zambia: a Prospective Clinical Cohort Study
Actual Study Start Date :
Aug 23, 2016
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Aug 1, 2024

Arms and Interventions

Arm Intervention/Treatment
HBV mono-infected (Standard of Care)

500 patients in Zambia

Other: Standard of care
Routine standard of care per Ministry of Health protocol, including blood draws and examinations.

Outcome Measures

Primary Outcome Measures

  1. Change in the percentage of patients with HBV viral suppression (Effectiveness of antiviral therapy in HBV-infected patients) [Baseline and after 1 year of treatment]

    The percentage of patients with HBV viral suppression.

Secondary Outcome Measures

  1. Proportion of chronic HBV-infected patients with an indication for antiviral treatment. [baseline, after 1 year of treatment, after 2 years of treatment]

    Using WHO HBV guidelines, the investigators will determine the proportion of chronic HBV infected patients in the cohort requiring antiviral treatment.

  2. HBV viral control among patients on antiviral treatment [baseline, after 1 year of treatment, after 2 years of treatment]

    The percentage of patients with viral control defined as undetectable HBV viral load after 1 and 2 years of treatment.

  3. Serologic, virologic, and hepatic features of chronic HBV infection in Zambia [0 to month 60]

    HBV patients' demographic characteristics at baseline and clinical characteristics at baseline and at 60 months, including alcohol use disorders diagnosed with AUDIT-C, HBV genotypes, HBV viral loads, prevalence of advanced liver disease (based on non-invasive tests), phase of HBV infection (immune tolerant, HBeAg-positive chronic hepatitis, HBeAg-negative chronic hepatitis, and immune control) - based on international guidance.

  4. Proportion with significant liver fibrosis [0, 12, 24, 36, 48, and 60 months,]

    Measure of liver fibrosis using AST-to-platelet ration index (APRI), Fibrosis 4 (FIB-4) and transient elastography.

  5. Incidence and prevalence of hepatocellular carcinoma (HCC) [baseline and after month 60]

    The number of new HCC cases (among those without evidence of HCC at baseline) divided by the time in the cohort study.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 99 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Age 18 years or older

  • HBV-infected, defined as any single positive HBsAg assay

Exclusion Criteria:
  • Unable or unwilling to provide informed consent

  • HIV-positive

Contacts and Locations

Locations

Site City State Country Postal Code
1 Tropical Gastroenterology and Nutrition Group Lusaka Zambia

Sponsors and Collaborators

  • University of Alabama at Birmingham
  • Tropical Gastroenterology and Nutrition Group
  • Centre for Infectious Disease Research in Zambia

Investigators

  • Principal Investigator: Michael J Vinikoor, MD, University of Alabama at Birmingham

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Michael Vinikoor, Assistant Professor, University of Alabama at Birmingham
ClinicalTrials.gov Identifier:
NCT03158818
Other Study ID Numbers:
  • F151224005
First Posted:
May 18, 2017
Last Update Posted:
Jun 2, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 2, 2022