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Clinical Trial Summary

This study will allow to assess liver related injuries in HIV patients.


Clinical Trial Description

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 ;


Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT02093754
Study type Interventional
Source French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (Inserm-ANRS)
Contact
Status Completed
Phase N/A
Start date May 2014
Completion date March 2016

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