HIV Infection Clinical Trial
Official title:
Assessing the Severity of Metabolic-related Liver Injuries in Aging HIV-monoinfected Patients: a European Multicentre Study
This study will allow to assess liver related injuries in HIV patients.
This study is a cross-sectional, multicentre study including 7 centres from 3 European
countries (Belgium, France, Germany).
The maximum duration of the study for each patient will be 4 months, consisting of:
- a screening visit,
- an inclusion visit to perform the biologic tests and exams necessary for the study,
within 1 month after the screening visit,
- a result delivery visit within 1 month after inclusion visit, to disclose results of
previous investigations. Patients with one or two non invasive markers suggesting
significant fibrosis (≥F2) will be invited for liver biopsy within the next 2 months.
- a "liver biopsy" visit, within 2 months after visit 2, liver biopsy in selected and
consented patients
;
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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