Non-Alcoholic Fatty Liver Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults aged 18 or older
- People who have been diagnosed with, or are suspected by a doctor to have, a liver condition called MASLD (a type of fatty liver disease)
- People with a body mass index (BMI) between 27 and 45 at the time of being referred to the study
- People who are able to lie still on a special device table for around 60 minutes
- People who are able to hold their breath repeatedly for about 20 seconds during scanning procedures
- People who are willing and able to take part in all parts of the study
Who may not be able to join:
- People who work for UCSD or Livivos as study staff
- People who have a medical reason why they cannot have an MRI scan (confirm with trial site)
- People who know they are pregnant, think they may be pregnant, or are trying to become pregnant
- People who have a known long-term liver disease other than MASLD
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Claude B Sirlin, MD, University of California, San Diego
Phone: 858-246-2198
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Agreement of LiverScope® measurements compared to conventional MR; Repeatability and reproducibility of LiverScope® measurements
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.