A simple body scan may spot fatty liver disease without needles
NCT ID NCT04873258
First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time
Summary
This study is testing whether a non-invasive tool, called bioimpedance vector analysis, can predict fatty liver disease (MASLD) in healthy volunteers. Researchers will use machine learning to analyze body composition data from about 2000 adults aged 18 to 80. The goal is to create a screening tool that could be used in clinical trials to identify liver issues without invasive procedures.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Bioimpedance vector analysis, a non-invasive test that measures body composition using a weak electrical current
- What this could lead to
- If successful, this could provide a quick, needle-free way to screen for fatty liver disease in clinical trial volunteers, replacing more invasive tests.
- What could go wrong
- The tool is still being developed and validated, so it may not prove accurate enough for widespread use. Early results may not apply to all populations.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 2,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2019
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult male or female volunteers for other clinical trials taking place at the study unit.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Male or female volunteers aged ≥18 to ≤80 years at the date of signing the informed consent. 2. 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. 3. 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: 1. GP diagnosis on HCF 2. Documented Fibroscan or liver US demonstrating MASLD Exclusion Criteria: 1. Known alcoholic liver disease, history of cirrhosis of any other cause (metabolic, viral hepatitis or other) 2. Any other significant previous liver pathology (liver malignancy, portal hypertension, infiltrative liver disease) 3. Alcohol consumption \>30 units per week 4. An Implanted cardiac devices
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Richmond Pharmacology Ltd. 1a Newcomen St, London Bridge
RECRUITINGLondon, London, SE1 1YR, United Kingdom
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