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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05264558
Other study ID # 16112020
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date July 25, 2022
Est. completion date September 30, 2023

Study information

Verified date November 2023
Source Macfarlane Burnet Institute for Medical Research and Public Health Ltd
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aims to assess the impact of models of HCV care on HCV testing, treatment uptake and cure within Cairns. Point of care testing for HCV , with test and treat strategies will be offered within a primary care service.


Description:

Available testing and treatment data will be explored pre and post the intervention period of the project within Cairns Hinterland health services that provide hepatitis C care. Test and treat strategies of the project will include: Part A: Same day test and treat clinical trial. The study will explore a 'same day test and treat' model to determine the impact on HCV treatment initiation and cure within a primary care service that recognises that they see people at risk of hepatitis C that are transient, and struggle to return to a care provider to engage in hepatitis C testing and care. 1. HCV RNA point of care (POC) testing 2. Epclusa (Sofosbuvir/Velpatasvir 400mg/100mg) course initiated at same day of visit following a +ve HCV RNA result from the POC test. Part B: Refresher and clinic in reach support work Primary care service/ General practitioner education and training ~1 hour in-person training for all clinic staff on hepatitis C testing, treatment, retention in HCV care cascade. Part C: Services evaluation with incentive and peer intervention in HCV care cascade.


Recruitment information / eligibility

Status Completed
Enrollment 606
Est. completion date September 30, 2023
Est. primary completion date August 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - attending primary health care service of CHHS aged 18 years or over Exclusion Criteria: only for intervention arm test and treat - Known to have hepatitis B or HIV infection - Known to have cirrhosis - Previous treatment with direct acting antivirals - Previously received interferon-based hepatitis C treatment that did not work - Women that are pregnant or breastfeeding - Already receiving hepatitis C treatment.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Xpert HCV Viral load finger stick point of care test (Cepheid)
Xpert HCV VL Fingerstick is an in vitro reverse transcription polymerase chain reaction (RT-PCR) assay for the detection and quantification of Hepatitis C Virus (HCV) RNA in human venous and capillary fingerstick EDTA whole blood. Appropriate pre and post testing counselling will be provided to participants.
Drug:
Epclusa 400Mg-100Mg Tablet
Same day HCV test and treatment
Other:
Standard of care
Clinical services will receive additional education and have the option of providing incentives to attendees of service.

Locations

Country Name City State
Australia Cairns and Hinterland Hospital and Health Service Cairns Queensland

Sponsors (3)

Lead Sponsor Collaborator
Macfarlane Burnet Institute for Medical Research and Public Health Ltd Cairns Hinterland Health Hospital and Health Services, The University of Queensland

Country where clinical trial is conducted

Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary HCV testing The number of participants who receive HCV testing in each of the arms 12 months
Primary HCV treatment The number of participants who start HCV treatment in each of the arms 12 months
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