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Clinical Trial Summary

Title Reaching out to the UNdiagnosed people infected with blood-borne viral infections (RUNtoBBV) Objectives 1. To study the efficacy of an outreach methodology to increase the uptake for screening, linkage to care and treatment in (active or former) people who use drugs (PWUD) Trial design Prospective multicenter interventional cohort design Number of subjects 336 inclusions (with prevalence of HCV Ab: 30%)

- 168 Antwerp

- 168 Limburg

Selection criteria Inclusion criteria:

- 18 years of age

- History of/ or active drug use

- Written informed consent obtained Exclusion criteria

- Currently enrolled in centralized OST program of Free Clinic or CAD Limburg Endpoints The following endpoints will be compared between the centers in Limburg and Antwerp: (Main outcome in bold)

Main objectives:

- Prevalence of blood-borne viral infections in Belgian (former or active) PWUD:

- HCV infection (number of HCV Ab+ / number of screened PWUD)

- HBV infection (number of HBsAg+/number of screened PWUD)

- HIV infection (number of HIV Ab+/number of screened PWUD)

- Analysis of linkage to care to hepatologist/ infectiologist (number of patients who adhered to their consultation/number of referred patients)

Secondary objectives:

- Analysis of risk behavior/sociodemographics linked to presence of BBV infections

- Analysis of uptake of anti(retro)viral treatment (number of patients started on treatment/number of patients needing treatment)

- Analysis of treatment adherence (adherence to treatment consultations/total planned consultations)

- Analysis of treatment outcome (total number of cured or virally suppressed patients/total number of treated patients)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04363411
Study type Interventional
Source Hasselt University
Contact
Status Completed
Phase N/A
Start date October 25, 2018
Completion date October 22, 2019

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