Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06387745

Referral of Patients to Hepatology With Hepatoscope

Led by University Hospital, Antwerp · Updated on 2026-05-08

200

Participants Needed

1

Research Sites

66 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Antwerp

Lead Sponsor

E

E-Scopics

Collaborating Sponsor

AI-Summary

What this Trial Is About

Patients identified as being at risk of liver fibrosis because of a positive Fibrosis-4 (FIB-4) test in the primary care setting will be offered be enrolled in the trial and to undergo an Hepatoscope exam (external non-invasive ultrasound imaging exam) to screen for liver fibrosis (with stiffness measurements) and/or steatosis (with ultrasound parameters related to fatty liver). All patients presenting with a liver stiffness value of at least 6.5 kilopascal (kPa) will be referred to the tertiary hepatology consultations for further assessment. Hepatoscope measurements will be compared to the standard of care for these patients, as defined at the tertiary hepatology center.

CONDITIONS

Official Title

Referral of Patients to Hepatology With Hepatoscope

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with elevated liver enzymes (AST, ALT, Gamma-GT, AP)
  • Patients with type 2 diabetes
  • Patients with elements of metabolic syndrome
  • Patients who provide written consent after oral information about the study
Not Eligible

You will not qualify if you...

  • Patients with active implants such as pacemakers, defibrillators, or pumps
  • Patients with wounds at the Hepatoscope probe placement site
  • Pregnant or breastfeeding women
  • People deprived of their freedom rights

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

Universitair Ziekenhuis Antwerpen

Edegem, Antwerp, Belgium, 2650

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SCREENING

Number of Arms

1

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