Evaluating Treatment as Prevention Among People Who Inject Drugs in Dundee for HCV
ERAPID HCV
1 other identifier
observational
2,800
1 country
1
Brief Summary
The aim of this study is to conduct an evaluation of hepatitis C treatments in NHS Tayside in order to empirically test the "treatment as prevention" models. This will be done by analysing the records of patients who have been tested and treated for hepatitis C using NHS Tayside databases. There will be no interventions carried out as part of this study.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2018
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 17, 2017
CompletedFirst Posted
Study publicly available on registry
November 29, 2017
CompletedStudy Start
First participant enrolled
April 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2024
CompletedApril 13, 2026
April 1, 2026
6.8 years
November 17, 2017
April 10, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
The number of HCV positive tests recorded in NHS Tayside.
The number of reactive DBST conducted in NHS Tayside.
6 years
Secondary Outcomes (3)
The number of patients engaged in treatment and SVR12 during the treatment phase
6 years
The cost of treatment
6 years
Re-infection with HCV following treatment
6 years
Eligibility Criteria
All individuals in NHS Tayside eligible for HCV testing and treatment according to Scottish Intercollegiate Guidelines Network guidelines.
You may qualify if:
- All individuals in NHS Tayside eligible for HCV testing and treatment according to Scottish Intercollegiate Guidelines Network guidelines.
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
NHS Tayside
Dundee, DD1 9SY, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 6 Years
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor John Dillon
Study Record Dates
First Submitted
November 17, 2017
First Posted
November 29, 2017
Study Start
April 1, 2018
Primary Completion
December 31, 2024
Study Completion
December 31, 2024
Last Updated
April 13, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share