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CompletedNCT03704792Updated Aug 8, 2022

Validation of the Second Generation of the Controlled Attenuation Parameter (CAP) Using the MRI-PDFF as Reference

An interventional study of FibroScan 530 Compact in Chronic Liver Disease, sponsored by Echosens. Completed at 5 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-08-08.

Sponsored by Echosens · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
207
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study summary

Chronic liver diseases (CLDs) represent a major worldwide public health burden. Worldwide estimations show that 844 million people have CLDs, a lot more than other chronic diseases such as diabetes or cardiovascular diseases. CLD is most of the time an asymptomatic, progressive, and potentially fatal disease. With its complications it becomes one of the major causes of mortality worldwide. Globally, hepatitis B virus and hepatitis C virus, alcoholic liver disease and non-alcoholic steatohepatitis, are the most important causes of liver disease.

The diagnosis of liver lesions remains an important issue for these patients. The prognosis and management of liver disease greatly depends on the amount of liver fibrosis. In early stages, it is the main factor predicting long-term outcome of these patients. The liver biopsy still represents the gold standard diagnostic tool for liver fibrosis assessment, although a wide spectrum of noninvasive tools are now commonly used as a surrogate to the liver biopsy. It includes direct and indirect serum markers of liver fibrosis, but also several imaging-based methods, including transient elastography (FibroScan®, Echosens, Paris, France).

Even if the liver fibrosis is the key pathological feature of progressive liver disease, the accumulation of excessive hepatic triglyceride, hepatic steatosis, is today recognized as an important factor in the pathogenesis of a number of CLD. The magnetic resonance imaging (MRI) techniques are sensitive to steatosis and show interesting diagnostic performances, especially the MRI using the proton density fat fraction (MRI-PDFF) which has shown at least equivalence in accuracy for quantifying hepatic steatosis with both 1H Magnetic Resonance Spectroscopy and with histological grade, across several studies. Therefore, this technique is now part of the gold standard diagnostic tool to establish the grade of hepatic steatosis. Echosens has developed an ultrasonic controlled attenuation parameter (CAP) designed to quantify hepatic steatosis using a process based on vibration controlled transient elastography (VCTE™).

Echosens is working on improving the diagnostic accuracy of the CAP measurement performed with the FibroScan. This protocol is set-up to compare the diagnostic performances of the first generation of the CAP and the second generation of the CAP to the reference, the MRI-PDFF, in patients with CLD, all etiologies combined.

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Conditions studied

  • Chronic Liver Disease

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In context

Liver Diseases

2,081 studies on the registry are indexed under Liver Diseases; 390 are open to participants now.

This study's enrollment of 207 is above the median of 50 across 1,323 interventional studies indexed under Liver Diseases.

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Lead sponsor

Echosens is the lead sponsor of 12 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patient must be at least 18 years of age
  • Patient must be able to give written informed consent
  • Patient affiliated to a social security system
  • Patient with a chronic liver disease, all etiologies

Exclusion criteria

Exclusion Criteria:

  • Vulnerable patient
  • Pregnant women
  • Patient with presence of ascites
  • Contra-indication to MRI
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
207 participants (actual)

Study arms

  • Experimental
    Adult CLD Group

    Only one group of patients in the study: adult patients with chronic liver disease (CLD), all etiologies combined, who will have a FibroScan 530 Compact examination to calculate the CAP value.

    Device: FibroScan 530 Compact

Interventions

  • DeviceFibroScan 530 Compact

    The FibroScan® is a device equipped with probes (M+ or XL+), each of which consists of an ultrasonic transducer mounted on the axis of a mechanical vibrator. Liver stiffness and CAP measurements are performed on the right lobe of the liver with the patient in a dorsal decubitus and maximal abduction position. The procedure is non-invasive and painless.

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What researchers measure

Primary outcomes

  1. Liver fat content assessed by MRI-PDFF.

    Time frame: 12 months

Secondary outcomes

  1. Ratio IQR CAPv1/CAPv2 and/or ratio standard deviation CAPv1/CAPv2

    Time frame: 12 months

  2. Difference between CAPv1 and CAPv2 measures

    Time frame: 12 months

  3. Correlation between CAPv1, CAPv2 and MRI-PDFF

    Time frame: 12 months

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Study locations

5 sites
  • Centre Hospitalier Universitaire d'Angers
    Angers, France
  • Hôpitaux Universitaires Paris Seine Saint-Denis - Service Hépatologie
    Bondy, 93140, France
  • Centre Hospitalier Universitaire de Bordeaux - Hôpital Haut Lévêque
    Bordeaux, France
  • Hôpital Saint-Antoine - Service Hépatologie
    Paris, 75012, France
  • CHU Rennes Hôpital Pontchaillou - Service des Maladies du Foie
    Rennes, 35033, France
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 8, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03704792
Lead sponsor
Echosens
Responsible party
Sponsor
First posted
Oct 15, 2018
Start date
Sep 24, 2019
Primary completion
Nov 30, 2021
Completion
Nov 30, 2021
Last update
Aug 8, 2022

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2022. You cannot join it, but the record below documents what was studied.

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