Sign in

NCT04873258Recruiting

Development of a Non-invasive Screening Tool to Predict Metabolic Dysfunction-associated Steatotic Liver Disease

Development of a Non-invasive Screening Tool to Predict Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD) in Volunteers on Clinical Trials Utilising Machine-learning and Bioimpedance Vector Analysis

Source: ClinicalTrials.gov · Last updated 19 Aug 2026

Brief summary (registry, in English)

A generic screening study to establish structural and/or functional baselines of specific organs.

Status (registry)
Recruiting
Study type
Observational
Enrollment
2000 (estimated)
First submitted
20 Apr 2021
Start date
27 Sept 2019
Primary completion date
31 Dec 2027
Lead sponsor
Richmond Research Institute
NCT number
NCT04873258

What you commit to

  • Study type: Observational
  • Planned participants: 2000
  • From 27 Sept 2019 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any other significant previous liver pathology (liver malignancy, portal hypertension, infiltrative liver disease)

Other illness

  • Known alcoholic liver disease, history of cirrhosis of any other cause (metabolic, viral hepatitis or other)
  • An Implanted cardiac devices

Other

  • Alcohol consumption \>30 units per week

Who the study is looking for

  • Male or female volunteers aged ≥18 to ≤80 years at the date of signing the informed consent.
  • Willingness and ability to provide written, personally signed, and dated informed consent, in accordance with the latest ICH Good Clinical Practice (GCP) Guidelines and applicable regulations.
  • An understanding, ability and willingness to fully comply with project procedures and restrictions.
    • For PART B only:
    • 1\. With a known history of MASLD as evidenced either of:
  • GP diagnosis on HCF
  • Documented Fibroscan or liver US demonstrating MASLD

Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Richmond Pharmacology Ltd. 1a Newcomen St, London Bridge
Coordinator of this site? Confirm its status
LondonUnited KingdomRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.