Randomised controlled trial conducted in injecting equipment provision sites to compare the effectiveness of different hepatitis C treatment regimens in people who inject drugs: A Direct obserVed therApy versus fortNightly CollEction study for HCV treatment-ADVANCE HCV protocol study.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
08 08 2019
Historique:
entrez: 11 8 2019
pubmed: 11 8 2019
medline: 2 9 2020
Statut: epublish

Résumé

Hepatitis C is a blood-borne virus (HCV) that can seriously damage the liver and is spread mainly through blood-to-blood contact with an infected person. Over 85% of individuals who have HCV in Scotland became infected following injecting drug use. Since people who inject drugs (PWID) are the main source of new infections, theoretical modelling has suggested that treatment of HCV infection in PWID may effectively reduce HCV prevalence and accomplish elimination. This protocol describes a clinical trial delivering HCV treatment within injecting equipment provision sites (IEPS) in Tayside, Scotland. PWID attending IEPS are tested for HCV and, if they are chronically infected with HCV and eligible, invited to receive treatment within the IEPS. They are randomised to one of three treatment regimens; daily observed treatment, treatment dispensed every 2 weeks and treatment dispensed every 2 weeks together with an adherence psychological intervention (administered before treatment begins). The primary outcome is comparison of the rate of successful treatment (SVR The ADVANCE (A Direct obserVed therApy versus fortNightly CollEction) HCV trial was given favourable opinion by East of Scotland Research Ethics Committee (LR/17/ES/0089) prior to commencement. European Clinical Trials Database (EudraCT) (2017-001039-38) and ClinicalTrials.gov (NCT03236506).

Identifiants

pubmed: 31399460
pii: bmjopen-2019-029516
doi: 10.1136/bmjopen-2019-029516
pmc: PMC6701606
doi:

Substances chimiques

Antiviral Agents 0

Banques de données

ClinicalTrials.gov
['NCT03236506']
EudraCT
['EudraCT2017-001039-38']

Types de publication

Clinical Trial Protocol Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e029516

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: SI, CB, AM, LB, ER, CS and KG have no competing interests. BS has has received honoraria for lectures from Abbvie, Janssen, Gilead, and MSD. JFD has received personal honoraria for lectures and instutional research grants from MSD, Abbvie, Gilead, Roche and Janssen.

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Auteurs

Sarah K Inglis (SK)

Tayside Clinical Trials Unit, University of Dundee, Dundee, UK s.k.inglis@dundee.ac.uk.

Lewis Jz Beer (LJ)

Tayside Clinical Trials Unit, University of Dundee, Dundee, UK.

Christopher Byrne (C)

Tayside Clinical Trials Unit, University of Dundee, Dundee, UK.

Amy Malaguti (A)

School of Social Sciences (Psychology), University of Dundee, Dundee, UK.

Emma Robinson (E)

Molecular and Clinical Medicine, University of Dundee, Dundee, UK.
Specialist liver service, NHS Tayside, Dundee, UK.

Christian Sharkey (C)

Specialist liver service, NHS Tayside, Dundee, UK.

Kirsty Gillings (K)

Psychology Department, NHS Fife, Cupar, UK.

Brian Stephens (B)

Specialist liver service, NHS Tayside, Dundee, UK.

John F Dillon (JF)

Molecular and Clinical Medicine, University of Dundee, Dundee, UK.
Specialist liver service, NHS Tayside, Dundee, UK.

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