Menu
Recruiting NCT07321925

Thermoacoustic Method for Estimating Liver Fat Fraction

— Observational MASLD/MASH (Metabolic Dysfunction-Associated Steatotic Liver Disease / Metabolic Dysfunction-Associated Steatohepatitis) Fatty Liver Disease, Nonalcoholic

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Thermoacoustic Enhanced Ultrasound.
Who it may be relevant to
Registry conditions: MASLD/MASH (Metabolic Dysfunction-Associated Steatotic Liver Disease / Metabolic Dysfunction-Associated Steatohepatitis), Fatty Liver Disease, Nonalcoholic. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Thermoacoustic Method for Estimating Liver Fat Fraction - Pilot Study I

Overview

The goal of this study is to use our Thermoacoustic Enhanced Ultrasound device to measure the fat levels in your liver and compare it to the the gold standard MRI PDFF measurements. Participants will have a scan with our device, then they will go have an abdominal MRI completed. The goal is to create a more accessible device to measure liver fat as it is an indicator for overall health and metabolic diseases.

Detailed description

The study will perform thermoacoustic fat measurements for up to 80 participants, over the span of the study. MRI-PDFF sequences will be acquired for participants in the study to establish a true measure of liver fat content, per the MRI gold standard. Determine the correlation between FLIP CID system Fat fraction results and the MRI-PDFF. Determine the accuracy between the fat measures obtained by the FLIP CID system participants who received a quantitative MRI. The following additional parameters will be evaluated endpoints: Sensitivity, Specificity ,Positive and negative predictive value (PPV, NPV) and The area under the ROC curve for the detection of liver fat abnormalities

Interventions

  • Device Thermoacoustic Enhanced Ultrasound
    a novel Thermoacoustic Enhanced imaging device

Primary outcome measures

  • Correlation between Thermoacoustic Fat Fraction (TAFF) and the MRI-PDFF [Time frame: From enrollment until the statistical analysis is reviewed, typically 2 weeks after last MRI data is received.]

Eligibility criteria

Inclusion criteria

  • Study participants are 18 or older.
  • Able to understand, read, and provide written informed consent in English.
  • Able to tolerate both ultrasound and MRI examinations.
  • Able to lie flat, or on their side, for 20 minutes and pause breathing for up to 10 seconds.

Exclusion criteria

  • Metal or electronic implants, including, but not limited to: pacemakers, metal clips, drug delivery pumps, hip implants, and neural stimulation devices, contraindicates for MRI.
  • Known pregnancy the day of consent or becoming pregnant during study participation based on start date of last menstrual period).
  • Liver diseases other than MASLD/MASH/fibrosis including, but not limited to:
  • Cirrhosis
  • Hepatocellular carcinoma
  • Ascites
  • Patients with broken, or injured skin, in the right upper abdominal quadrant.
  • Body habitus, or anatomical variation, where the liver capsule is not accessible with ultrasound through the patient's right intercostal imaging window used in conventional ultrasound liver imaging.
  • BMI greater than 50 kg/m2
  • Patients with subcutaneous fat at measurement location less than or equal to 6mm.
  • Patients with a missing liver lobe.
  • Patients with peri-hepatic fat in the measurement location.
  • Patients with focal liver lesions or anatomical structures in the measurement location, as detected by ultrasound.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

United States · 1 center
  • ENDRA Life Sciences — Ann Arbor

Identifiers

NCT: NCT07321925 · ENDRA-CL25-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗