Opportuni-C: Opportunstic Hepatitis C Virus Treatment

Sponsor
University Hospital, Akershus (Other)
Overall Status
Unknown status
CT.gov ID
NCT04220645
Collaborator
(none)
200
1
2
12
16.7

Study Details

Study Description

Brief Summary

The project will assess the effect of opportunistically treating hepatitis C virus (HCV) infection immediately when HCV-infected people who inject drugs are hospitalized for acute care in psychiatric, interdisciplinary specialized drug treatment or somatic wards. We will compare this approach with the current standard of care (SOC), which is referral to the outpatient clinic at the medical department following discharge.

Condition or Disease Intervention/Treatment Phase
  • Other: Opportunstic treatment
  • Other: Standard of care
N/A

Detailed Description

The overall objective is to show that opportunistic and immediate administration of HCV treatment is more efficient compared to referral-based SOC. The specific objectives are: 1) to compare the intervention and SOC groups with regards to treatment completion, treatment uptake and virologic response ; 2) to assess the rate of reinfection after successful HCV treatment; and 3) to assess the frequency of resistant associated substitutions before and after virologic treatment failure.

We will use a stepped wedge design and include patients in 7 clusters

Following randomization of the cluster to the immediate treatment, physicians at the participating wards will be notified in writing that for the next time period patients diagnosed with HCV infection should be treated immediately. In addition, lectures presenting the opportunistic approach will be given and the Department of Microbiology will add a brief text to the result of HCV RNA testing reminding about the opportunistic approach. In the medical and the psychiatric departments, consultants from the departments of infectious diseases or gastroenterology will prescribe immediate treatment. In the departments that provide addiction treatment, local physicians will prescribe treatment. Treatment will be prescribed in accordance with current Norwegian treatment recommendations. The intensity of care after discharge will be individualized at the discretion of the treating physician.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Pragmatic clinical trial. Cluster randomised with stepped wedge designPragmatic clinical trial. Cluster randomised with stepped wedge design
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Opportunistic Treatment of Hepatitis C Virus Infection (OPPORTUNI-C): A Pragmatic Clinical Trial of Immediate Versus Outpatient Treatment Initiation Among Hospitalized Patients
Actual Study Start Date :
Oct 1, 2019
Anticipated Primary Completion Date :
Sep 30, 2020
Anticipated Study Completion Date :
Sep 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Standard of care

Hospitalised patients with hep C are referred to the outpatient clinic at the medical department following discharge.

Other: Standard of care
Referral at discharge

Experimental: Opportunistic treatment

Hospitalised patients with hep C are opportunistically and immediately treated when hospitalized for acute care in psychiatric, addiction treatment or somatic wards

Other: Opportunstic treatment
opportunistically treating HCV infection immediately when hep C patients are hospitalized for acute care in psychiatric, addiction treatment or somatic wards

Outcome Measures

Primary Outcome Measures

  1. Treatment completion [12 weeks]

    Proportion in each arm who have been dispensed the last 28 days package of HCV treatment

Secondary Outcome Measures

  1. Sustained virological response [24 weeks]

    HCV RNA undetetctable 12 weeks after end of treatment

  2. Reinfection [Two years]

    A HCV RNA strain not present at baseline is detected during or after treatment

  3. End of treatment response [12 weeks]

    Proportion in each arm who have undetectable HCV RNA at the end of treatment

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

Inclusion criteria

  • Above 18 years of age

  • HCV RNA positive

  • Inpatient at participating ward

  • Signed informed consent must be obtained and documented according to national and local regulations

Exclusion criteria:
  • Pregnancy or breastfeeding.

  • In involuntarily health care.

  • Ongoing treatment of hepatitis C.

  • Current participation in another trial that might affect the current study.

  • Any reason why, in the opinion of the investigator, the patient should not participate (e.g. not able to comply with study procedures).

Contacts and Locations

Locations

Site City State Country Postal Code
1 AkershusUH Lørenskog Select A State Or Province Norway 0278

Sponsors and Collaborators

  • University Hospital, Akershus

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Olav Dalgard, Professor, University Hospital, Akershus
ClinicalTrials.gov Identifier:
NCT04220645
Other Study ID Numbers:
  • 2019/128
First Posted:
Jan 7, 2020
Last Update Posted:
Jan 7, 2020
Last Verified:
Jan 1, 2020
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
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 7, 2020