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NCT Number: NCT06661655

Evaluation of a New Ultrasound System for the Non-invasive Assessment of Liver Steatosis in MASLD/MASH Patients

The objective of the study is to evaluate an ultraportable ultrasound device, Hepatoscope, for the non-invasive assessment of hepatic steatosis in patients with metabolic-dysfunction associated liver diseases (MASLD), by comparing its measurements with current diagnostic modalities, such as MRI-PDFF.

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Key information

About this study

The objective of the study is to evaluate an ultraportable ultrasound device, Hepatoscope, for the non-invasive assessment of hepatic steatosis in patients metabolic-dysfunction associated liver diseases (MASLD), by comparing its measurements with current diagnostic modalities, such as MRI PDFF.

The primary objective is to compare ultrasound parameters measurements of ultrasound attenuation, backscattering coefficient and sound speed to the hepatic fat fraction as measured with MRI-PDFF.

The secondary objectives includes the comparison of measurements of quantitative ultrasound parameters between Hepatoscope and FibroScan, and to compare the measurement of liver stiffness between Hepatoscope and MRE.

Exploratory objectives have been determined to allow the comparison of said measured parameters to the outcome of histopathological analysis in a subset patient population who would benefit from a liver biopsy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patient below 80 yo
  • Patients with MASLD/MASH recruited in interventional trials requiring MRI PDFF +/- MRE per interventional protocol, OR
  • Patients with MASLD/MASH recruited in prospective cohorts requiring MRI PDFF +/- MRE per interventional protocol, OR
  • Patients referred to MRI-PDFF or MRE.
  • Patients who consented in written to participate in the study
  • Patients with ongoing social security coverage

Exclusion criteria

  • Patient in their minority (less than 18 yo) or older than 80 yo,
  • Patient with active implants,
  • Patient presenting with a wound where the Hepatoscope exam shall be performed (abdominal right upper quadrant)
  • Patient with a history of decompensated cirrhosis,
  • Patient with a history of hepatocellular carcinoma,
  • Adult patient under tutorship, or unable to express informed consent,
  • Pregnant or breast-feeding
  • Person deprived from their liberty
  • Patient hospitalized without providing consent or in case of an emergency
  • Patient presenting with another know liver disease

Treatment and study plan

Liver ultrasound

Device

Hepatoscope is a point of care ultraportable ultrasound device that is capable of conventional grayscale ultrasound imaging, of 2D transient elastography (imaging + liver stiffness measurement), and of quantitative ultrasound properties measurement (ultrasound attenuation, backscattering coefficient, sound speed) related to liver steatosis.

Primary outcomes

  1. Correlation with MRI PDFF

    Time frame: At a maximum of 6 months from enrollment

    Spearman correlation coefficients between each Hepatoscope measurement (ATT, BSC and SOS) and MRI-PDFF measurements will be calculated. The confidence interval will be estimated with an alpha risk of 0,017 (Bonferroni adjustment, overal alpha risk of 0,05). Each correlation will be compared to the lowest acceptable threshold D = 0,50 with a Fisher Z test, with an alpha risk de 0,017.

Secondary outcomes

  1. Comparison with Fibroscan CAP

    Time frame: At a maximum of 6 months from enrollment

    Spearman correlations between Hepatoscope measurements and MRI-PDFF will be compared to Spearman correlations between Fibroscan CAP measurements and MRI-PDFF. The 95% confidence interval of each correlation will be estimated and compared to each other using a Fisher Z test with an alpha risk of 0,05.

Study contacts

Contact information is provided by the study sponsor or research team.

Jerome Boursier, MD, PhD

CONTACT

[email protected]

+33 2 41 35 31 42

Sponsors and collaborators

Lead sponsor

E-Scopics

Industry

Registry information

Acronym: ACOUSTIQ

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Oct 28, 2024
Registry last updated
Aug 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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