New portable MRI could spot fatty liver in minutes
NCT ID NCT05986916
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study is testing a new portable device called LiverScope that uses MRI-like technology to measure fat in the liver. Researchers will compare it to standard MRI and FibroScan in 50 adults with known or suspected non-alcoholic fatty liver disease (NAFLD). Participants undergo a one-time visit with scans and a blood draw. The goal is to see if LiverScope can reliably diagnose liver fat without needing a full hospital MRI.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- LiverScope® exam (portable MRI device)
- What this could lead to
- If successful, this could provide a simpler, more accessible way to diagnose and monitor fatty liver disease without needing large hospital MRI machines.
- What could go wrong
- This is a small, early-stage study (50 participants) focused on comparing measurements, not on treatment. The device is not yet approved for clinical use, and results may not apply to all patients.
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
-
About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Aug 2023
- Expected to finish
-
Nov 2025
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adults with clinically known or suspected liver disease.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Age:18 years or older * Known or clinically suspected NAFLD * Weight less than 350 lbs (safety limit of MR scanner table) * Able to lie on LiverScope® diagnostic table for about 15 min * Able to hold breath repeatedly for about 20 s during MR and LiverScope® exams * Willing and able to undergo all study procedures Exclusion Criteria: * VA patient only; not a UCSD patient * UCSD or Livivos study personnel * MR contraindication(s) * Potential participant states that she knows that she is pregnant, thinks she may be pregnant or states she is trying to become pregnant\* * Known chronic liver disease other than NAFLD
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for NAFLD are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
Contacts and locations
Locations
-
University of California San Diego
La Jolla, California, 92037, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can talk therapy and mindfulness shrink a fatty liver?
- A smartphone app may help curb the silent march of fatty liver disease toward cirrhosis
- AI and blood biomarkers could catch hidden liver damage
- A protein supplement may fight fatty liver in teens
- Can a single pill tackle both fatty liver and diabetes?
- Could immune cells in fat hold the key to Obesity-Related diseases?