Prospective Single Centre Observational Study to Compare the Diagnostic Yield of Different Modalities of Liver Biopsy
NCT ID: NCT05912179
Last Updated: 2023-06-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
200 participants
OBSERVATIONAL
2022-09-01
2023-09-30
Brief Summary
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The main questions it aims to answer are:
1. is EUS liver biopsy equally as good as other types of techniques
2. are there any advantages to using the EUS technique to obtain liver biopsies Researchers will compare data from patients who have had a liver biopsy with a traditional technique with those who have undergone EUS-guided biopsy.
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Detailed Description
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The rising incidence of liver disease (LD) has led to an increased demand on services for accurate and prompt diagnosis and staging, to facilitate treatments and early interventions. While non-invasive diagnostic tests (e.g. transient elastography, ELF biomarkers) are the standard of care to stratify fibrosis burden, there are still cases that require a liver biopsy (LB) for assessment of fibrosis and aetiology of disease. Traditional methods such as percutaneous LB (PLB) and transjugular LB (TJLB) are well established, however there is a recognised burden on the services, translating to prolonged waiting times and delays in diagnosis. Endoscopic ultrasound-guided liver biopsy (EUS-LB) is emerging as a novel, minimally invasive way of not only securing a tissue sample, but also providing an in-depth assessment of other parameters such as portal pressure gradient (PPG), shearwave measurement (SWM) and varices assessment. The aim of this study was to test the diagnostic adequacy, fibrosis staging, length of stay post procedure and complication rates following the above modalities of Liver biopsy.
Methods:
This is a single centre prospective observational study to assess the diagnostic accuracy of liver biopsy through different modalities. Data will be as collected prospectively from all adult patients patients undergoing any form of LB in a single tertiary hospital for 12 months:September 2022 to September 2023. Information was collected will be on demographics, biopsy indication, length of core, length of stay (LoS), complications and diagnostic yield.
Primary aim: To assess the diagnostic yield of liver biopsy through EUS-LB, Trans-jugular liver biopsy and percutaneous ultrasound guided liver biopsy.
Secondary aim;
1. Technical success rate,
2. Length of the cores obtained
3. Number of portal tracts
4. Accuracy of Shear wave measurement compared to Liver biopsy
5. complications rate
6. Length of stay
Dissemination plan:
the results of the study will be disseminated through presentation at national/ international meetings and publishing in peer reviewed journals.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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EUS guided liver biopsy
Patients having liver biopsy through endoscopic ultrasound technique
liver biopsy - EUS guided
liver biopsy obtained during endoscopic ultrasound
Percutaneous liver biposy
Patients having liver biopsy percutaneously
Liver biopsy - percutaneous
liver biopsy obtained using percutaneous ultrasound guided technique
Transjugular liver biopsy
Patients having liver biopsy via a transjugular route
Liver biopsy - transjugular
liver biopsy obtained using an interventional transjugular approach
Interventions
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Liver biopsy - percutaneous
liver biopsy obtained using percutaneous ultrasound guided technique
Liver biopsy - transjugular
liver biopsy obtained using an interventional transjugular approach
liver biopsy - EUS guided
liver biopsy obtained during endoscopic ultrasound
Eligibility Criteria
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Inclusion Criteria
* underwent liver biopsy either through EUS, percutaneous or transjugular route
Exclusion Criteria
18 Years
100 Years
ALL
Yes
Sponsors
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Nottingham University Hospitals NHS Trust
OTHER
Responsible Party
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Suresh Vasan Venkatachalapathy
Consultant Hepatologist
Principal Investigators
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Suresh Vasan Suresh Vasan
Role: PRINCIPAL_INVESTIGATOR
Nottingham University Hospitals
Locations
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Nottingham University Hospitals NHS Trust
Nottingham, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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22-577C
Identifier Type: -
Identifier Source: org_study_id
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