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

NCT03704792 | Completed

• 1 other identifier: M134
• Study Type: interventional
• Target: 207
• Locations: 1 country
• Sites: 5

Brief 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.

Conditions

Chronic Liver Disease

Outcome Measures

Primary Outcomes (1)

• Liver fat content assessed by MRI-PDFF.

  12 months

Secondary Outcomes (3)

• Ratio IQR CAPv1/CAPv2 and/or ratio standard deviation CAPv1/CAPv2

  12 months

• Difference between CAPv1 and CAPv2 measures

  12 months

• Correlation between CAPv1, CAPv2 and MRI-PDFF

  12 months

Study Arms (1)

Adult CLD Group

EXPERIMENTAL

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

FibroScan 530 Compact DEVICE

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.

Adult CLD Group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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

You may not qualify if:

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

Sponsors & Collaborators

• Echosens: lead

Study Sites (5)

Centre Hospitalier Universitaire d'Angers

Angers, France

Location

Hôpitaux Universitaires Paris Seine Saint-Denis - Service Hépatologie

Bondy, 93140, France

Location

Centre Hospitalier Universitaire de Bordeaux - Hôpital Haut Lévêque

Bordeaux, France

Location

Hôpital Saint-Antoine - Service Hépatologie

Paris, 75012, France

Location

CHU Rennes Hôpital Pontchaillou - Service des Maladies du Foie

Rennes, 35033, France

Location

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: DIAGNOSTIC
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 10, 2018
• First Posted: October 15, 2018
• Study Start: September 24, 2019
• Primary Completion: November 30, 2021
• Study Completion: November 30, 2021
• Last Updated: August 8, 2022

Record last verified: 2022-08

Locations

FR (5)