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

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-09-01

Study Completion Date

2023-09-30

Brief Summary

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The goal of this study is to learn about endoscopic ultrasound(EUS) guided liver biopsy and how this compares to traditional methods of obtaining liver biopsy samples, in patients with liver disease.

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.

Detailed Description

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Introduction:

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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Liver Diseases Liver Fibrosis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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EUS guided liver biopsy

Patients having liver biopsy through endoscopic ultrasound technique

liver biopsy - EUS guided

Intervention Type DIAGNOSTIC_TEST

liver biopsy obtained during endoscopic ultrasound

Percutaneous liver biposy

Patients having liver biopsy percutaneously

Liver biopsy - percutaneous

Intervention Type DIAGNOSTIC_TEST

liver biopsy obtained using percutaneous ultrasound guided technique

Transjugular liver biopsy

Patients having liver biopsy via a transjugular route

Liver biopsy - transjugular

Intervention Type DIAGNOSTIC_TEST

liver biopsy obtained using an interventional transjugular approach

Interventions

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Liver biopsy - percutaneous

liver biopsy obtained using percutaneous ultrasound guided technique

Intervention Type DIAGNOSTIC_TEST

Liver biopsy - transjugular

liver biopsy obtained using an interventional transjugular approach

Intervention Type DIAGNOSTIC_TEST

liver biopsy - EUS guided

liver biopsy obtained during endoscopic ultrasound

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* 18 years or older
* underwent liver biopsy either through EUS, percutaneous or transjugular route

Exclusion Criteria

\- under 18 years of age
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Nottingham University Hospitals NHS Trust

OTHER

Sponsor Role lead

Responsible Party

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Suresh Vasan Venkatachalapathy

Consultant Hepatologist

Responsibility Role PRINCIPAL_INVESTIGATOR

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

Site Status RECRUITING

Countries

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United Kingdom

Central Contacts

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Suresh Vasan Venkatachalapathy

Role: CONTACT

07966968417

Facility Contacts

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Suresh V Venkatachalapathy, MRCP

Role: primary

01159249924 ext. 70441

Other Identifiers

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22-577C

Identifier Type: -

Identifier Source: org_study_id

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