Opportuni-C: Opportunstic Hepatitis C Virus Treatment
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 |
---|---|---|
|
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
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
- Treatment completion [12 weeks]
Proportion in each arm who have been dispensed the last 28 days package of HCV treatment
Secondary Outcome Measures
- Sustained virological response [24 weeks]
HCV RNA undetetctable 12 weeks after end of treatment
- Reinfection [Two years]
A HCV RNA strain not present at baseline is detected during or after treatment
- End of treatment response [12 weeks]
Proportion in each arm who have undetectable HCV RNA at the end of treatment
Eligibility Criteria
Criteria
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.- 2019/128