HepC:CAC: Evaluating the Chain of Addiction Care (CAC)

Sponsor
Radboud University Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT05401136
Collaborator
AbbVie (Industry), Gilead Sciences (Industry)
1,000
1
45
22.2

Study Details

Study Description

Brief Summary

The investigators want to evaluate the feasibility of a decentralised hepatitis C care pathway (the Chain of Addiction Care (CAC) pathway) in several addiction care centres in the east of the Netherlands. Secondary objective: to measure the impact of hepatitis C clearance on MET (+metabolite) and BUP (+metabolite) trough levels in patients on Opioid substitution Therapy (OST). This is an exploratory, observational study.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    People who (have) inject(ed) drugs (PWID) are at high risk for hepatitis C infection. Establishing adequate linkage to care in this population can be a challenge. Many of these patients receive opioid substitution, hepatitis C treatment possibly influences pharmacokinetics of those substitutes. This protocol describes a study on hepatitis C in people who (have) inject(ed) drugs (PWID), consisting of two substudies. 1) An exploratory, observational study in which we evaluate the decentralised hepatitis C care pathway in addiction care centres. 2) An observational pharmacokinetic study in hepatitis C patients on opioid substitution therapy (OST) embedded within the first study.

    Rationale: 1) Many PWIDs are lost during the process of testing and linkage to care and do therefore not receive adequate hepatitis C treatment. Decentralising care in addiction care centres deems hospital visits unnecessary, an approach that has become increasingly popular in this population over the last few years. This practice however has not yet been evaluated in the Netherlands. 2) In the Netherlands the PWID population is often treated for opioid addiction by opioid substitution therapy (OST) with methadone (MET) or buprenorphine (BUP). There is evidence that liver inflammation has a negative effect on pharmacokinetics of drugs. Consequently, we hypothesize that HCV treatment results in reduced liver inflammation and a decrease in MET and/or BUP levels, which is clinically relevant in the PWID/OST population.

    Objective: 1) to evaluate the feasibility of a decentralised hepatitis C care pathway (the Chain of Addiction Care (CAC) pathway) in several addiction care centres in the east of the Netherlands. 2. to measure the impact of hepatitis C clearance on MET (+metabolites) and BUP (+metabolites) levels and craving in patients on OST.

    Study design: This is an exploratory, observational study with a pharmacokinetic observational study embedded within the same population.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    1000 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Evaluating the Hepatitis C Chain of Addiction Care Pathway for People Who Inject(ed) Drugs in Addiction Care
    Actual Study Start Date :
    Mar 1, 2020
    Anticipated Primary Completion Date :
    Dec 1, 2023
    Anticipated Study Completion Date :
    Dec 1, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    Participants

    Consecutive people who use drugs and visit the addiction care centre

    Outcome Measures

    Primary Outcome Measures

    1. HCV prevalence (both anti-HCV and HCV RNA). [At screening (week 0)]

      Participants are invited to undergo viral hepatitis screening (standard care)

    2. Treatment acceptance rate. [After evaluation (~week 3)]

      Participants with chronic HCV infection are invited to be treated (standard care)

    3. Sustained virologic response [12 weeks after treatment (~week 30)]

      Participants who were treated and were 'cured' (standard care)

    Secondary Outcome Measures

    1. Acceptance rate of on-site testing. [through study completion, an average of 1 year]

      Number of participants that engage in testing

    2. Re-infection rate. [through study completion, an average of 1 year]

      Patients re-infected after successful treatment

    3. Mean decrease in MET and BUP trough levels [through study completion, an average of 1 year]

      Difference in concentration of methadone or buprenorphine before and after treatment.

    4. Change in dosage of MET and BUP during follow-up [through study completion, an average of 1 year]

      Physician initiated dosage change before compared to after treatment of hepatitis C

    5. Patient reported drug use [through study completion, an average of 1 year]

      Drug use during study timeframe

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Aged 18 years or older

    • Able and willing to give informed consent

    • Currently inject or previously injected drugs at least once, including nasal snorting of drugs using aids such as basepipes or straws.

    • Visit the participating addiction care centre at least once during the study period

    Exclusion Criteria:
    • none

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Radboudumc Nijmegen Gelderland Netherlands 6525GA

    Sponsors and Collaborators

    • Radboud University Medical Center
    • AbbVie
    • Gilead Sciences

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Radboud University Medical Center
    ClinicalTrials.gov Identifier:
    NCT05401136
    Other Study ID Numbers:
    • 2019-5939
    First Posted:
    Jun 2, 2022
    Last Update Posted:
    Jun 2, 2022
    Last Verified:
    May 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 2, 2022