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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT02000063
Registration number
NCT02000063
Ethics application status
Date submitted
12/11/2013
Date registered
3/12/2013
Date last updated
1/10/2014
Titles & IDs
Public title
Australian Trial in Acute Hepatitis C Recall Study
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Scientific title
Long-term Outcomes Following Treatment of Recently Acquired Hepatitis C Virus Infection.
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Secondary ID [1]
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VHCRP1105
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Secondary ID [2]
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VHCRP1105
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Universal Trial Number (UTN)
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Trial acronym
ATAHC Recall
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Acute Hepatitis C
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Condition category
Condition code
Infection
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Other infectious diseases
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Oral and Gastrointestinal
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Long-term effects of HCV clearance
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Assessment method [1]
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Health related quality of life (measured by SF-12) Social functioning (measured by OTI survey) Injecting behaviour Mental health (measured by DASS and MINI) Liver health (measured by FibroScan and biochemical markers)
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Timepoint [1]
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4 to 8 years from initial infection
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Secondary outcome [1]
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Incidence of HCV re-infection
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Assessment method [1]
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Rate of HCV RNA positivity in patients previously HCV RNA negative.
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Timepoint [1]
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4 to 8 years from initial infection
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Eligibility
Key inclusion criteria
* Previous enrolment in the Australian Trial of Acute Hepatitis C Virus Infection (ATAHC) Study.
* Provision of written, informed consent.
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Minimum age
16
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* In the opinion of the investigator that the patient is not able to provide informed consent.
* Inability or unwillingness to comply with study collection requirements.
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/08/2012
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/03/2014
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Sample size
Target
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Accrual to date
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Final
50
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Recruitment in Australia
Recruitment state(s)
NSW,SA,VIC
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Recruitment hospital [1]
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St Vincent's Hospital - Sydney
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Recruitment hospital [2]
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Royal Adelaide Hospital - Adelaide
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Recruitment hospital [3]
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The Alfred Hospital - Melbourne
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Recruitment postcode(s) [1]
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2010 - Sydney
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Recruitment postcode(s) [2]
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5000 - Adelaide
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Recruitment postcode(s) [3]
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3005 - Melbourne
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Funding & Sponsors
Primary sponsor type
Government body
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Name
Kirby Institute
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Address
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Country
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Other collaborator category [1]
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Other
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Name [1]
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The University of New South Wales
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
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Summary
Brief summary
A single long-term follow up assessment of an established multi-centre, prospective longitudinal cohort study of patients for clinical, psychosocial, immunovirological outcomes 4 to 8 years after previous treatment for recently acquired hepatitis C virus infection.
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Trial website
https://clinicaltrials.gov/study/NCT02000063
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Gail Matthews, MBChB, MRCP (UK), FRACP, PhD
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Address
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University of New South Wales, Syndey Australia
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT02000063
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