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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06047275
Other study ID # RS193 - 323660
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date May 1, 2023
Est. completion date May 31, 2024

Study information

Verified date September 2023
Source University of Hull
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Hepatitis C diagnostic devices have been developed at the University of Hull to detect and quantify the Hepatitis C virus in patients' plasma and serum samples. This study aims to test the new point-of-care devices that are designed to be low cost and user-friendly. Excess, stored, HCV patients' plasma, serum and blood samples will be supplied by the Virology laboratory (Hull University Teaching Hospital's Trust; HUTH). These samples were taken and analysed as part of patients' clinical monitoring, and are stored prior to disposal in the Virology laboratory. The proposed study will use the samples in a fully anonymised manner.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 20
Est. completion date May 31, 2024
Est. primary completion date May 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Blood sample taken Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom University of Hull Kingston upon Hull

Sponsors (2)

Lead Sponsor Collaborator
University of Hull Hull University Teaching Hospitals NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Positivity Paper microfluidic test 30 min
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