Actively Recruiting

Age: 18Years - 100Years
All Genders
NCT05541601

Prospective Cohort for Early Detection of Liver Cancer

Led by University of Oxford · Updated on 2022-09-15

3000

Participants Needed

1

Research Sites

801 weeks

Total Duration

On this page

Sponsors

U

University of Oxford

Lead Sponsor

C

Cancer Research UK

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study aims to recruit 3000 people with liver cirrhosis into a Prospective cohort for early detection of Liver cancer - the Pearl cohort. The study team believe that using a combination of novel tests may improve the detection of early Hepatocellular Carcinoma (HCC).

CONDITIONS

Official Title

Prospective Cohort for Early Detection of Liver Cancer

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients of all genders aged over 18 years
  • Able and willing to give informed consent to participate
  • Diagnosed with cirrhosis Child-Pugh Class A or B
  • Cirrhosis caused by chronic Hepatitis B or C infection, alcoholic liver disease, non-alcoholic fatty liver disease, or haemochromatosis
  • Cirrhosis diagnosis confirmed by histology or validated non-invasive markers, varices evidence, or radiological signs of cirrhosis
Not Eligible

You will not qualify if you...

  • Current or past diagnosis of hepatocellular carcinoma
  • Liver transplant recipients or those actively listed for transplantation
  • Cirrhosis classified as Child-Pugh Class C
  • Serious co-morbid conditions likely to cause death within 12 months as judged by a clinician
  • Considered unsuitable for HCC surveillance by a clinician

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hepatology Clinical Trial Unit, John Radcliffe Hospital

Oxford, Oxfordshire, United Kingdom, OX3 9DU

Actively Recruiting

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Research Team

S

Study Coordinator

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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