Prevention of primary liver cancer with selenium supplementation - targeted to high risk population Cancer Liver cancer
Conditions
Interventions
Eligible patients who consent to participate will be randomly allocated to the selenium group (oral selenium supplementation: 200mg selenium per day, in the form of selenized yeast tablet) or control
Sponsors
The University of Birmingham (UK)
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: Participants will include: 1. Men aged 45 to 64 with positive HBsAg (hepatitis B surface antigen) test 2. Negative AFP (alphafetoprotein) test 3. Normal ALT (alanine aminotransferase) values
Exclusion criteria
Exclusion criteria: Not provided at time of registration
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Secondary
| Measure | Time frame |
|---|---|
| Not provided at time of registration | — |
Countries
United Kingdom
Outcome results
None listed