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NCT04681573Recruiting

Comparison of Two sTRAtegies For the Non-Invasive Diagnosis of advanCed Liver Fibrosis in NAFLD

Source: ClinicalTrials.gov · Last updated 18 Nov 2025

Brief summary (registry, in English)

NAFLD, closely linked to overweight and insulin resistance, has reached 25% prevalence worldwide. Advanced liver fibrosis(ALF) must be accurately diagnosed in NAFLD because it defines a subgroup of patients with impaired prognosis, and these patients need a specific management to prevent the occurrence of liver-related complication. Relatively few NAFLD patients develop ALF and it is a challenge for physicians to identify them. Liver biopsy is the reference for liver fibrosis evaluation but this invasive procedure cannot be first-line used in NAFLD. Non-invasive diagnosis of liver fibrosis is now available, especially liver stiffness measurement (LSM) with Fibroscan and blood fibrosis tests. However, Fibroscan is a costly device available only in few specialized centres with thus poor accessibility in face of the large NAFLD population. Blood fibrosis tests can be performed by every physician and are distinguished as "complex" or "simple". Because they include specialized biomarkers, complex blood fibrosis tests are accurate for the diagnosis of ALF but they are quite expensive and not reimbursed, with therefore limited use in clinical practice. Simple blood fibrosis tests have the advantage to include cheap and easy-to-obtain biomarkers with simple calculation thanks to free websites or smartphone applications. Simple blood fibrosis tests are globally less accurate than complex blood fibrosis tests or Fibroscan but, used with a high-sensitivity cut-off, they have the high interest of being able to accurately rule out advanced fibrosis in a significant proportion of NAFLD patients. Recently, two sequential diagnostic procedures have been developed for the diagnosis of ALF with the idea to combine the advantages of the different kind of fibrosis tests: the FIB4-Fibroscan (FIB4-FS) and the eLIFT-FibroMeterVCTE (eLIFT-FMVCTE) algorithms. These algorithms include as first-line procedure a simple blood fibrosis test (FIB4 or eLIFT) which identifies the patients who require a further second-line evaluation with a more accurate non-invasive test (Fibroscan or FibroMeterVCTE). Liver biopsy is finally used as third-line procedure in patients for whom the diagnosis remains undetermined. Such algorithms have the advantage to limit the use of complex fibrosis tests only to a subset of at risk-patients. The TRAFIC study compare two strategies for the diagnosis of ALF in NAFLD patients: the FIB4-Fibroscan algorithm and the eLIFT-FibroMeterVCTE algorithm

Status (registry)
Recruiting
Study type
Interventional
Enrollment
1045 (estimated)
First submitted
11 Dec 2020
Start date
7 Apr 2022
Primary completion date
7 Oct 2028
Lead sponsor
University Hospital, Angers
NCT number
NCT04681573

What you commit to

  • Study type: Interventional
  • Planned participants: 1045
  • From 7 Apr 2022 to the primary completion date, 7 Oct 2028
  • 20 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participation in other intervention study with drug protocol treatment in progress at the time of inclusion or within one month prior to inclusion in the study.

Other illness

  • Decompensated cirrhosis (ascites, variceal bleeding, hepatic encephalopathy, liver failure, hepato-renal syndrome)
  • Person under psychiatric care under restraint

Other

  • Hepatocellular carcinoma
  • Inability to safely undergo liver biopsy
  • Pregnant, breastfeeding or parturient woman
  • Person restricted by judicial or administrative decision
  • Person subject to a legal protection measure
  • Person unable to express consent

Who the study is looking for

  • Presence of NAFLD as defined by :
    • The presence of liver steatosis as assessed by ultrasonography (bright liver) or magnetic resonance imaging/spectroscopy (fat fraction \>5.6%) or Controlled Attenuation Parameter (≥248 dB/m)
    • The absence of steatosis-inducing drugs (systemic corticosteroids, methotrexate, amiodarone, tamoxifen)
    • The absence of excessive alcohol consumption (\<210 g/week in men or \<140 g/week in women)
    • The absence of other causes of chronic liver disease (chronic viral hepatitis B or C, hemochromatosis, auto-immune hepatitis, primary biliary cholangitis, primary sclerosing cholangitis, Wilson disease alpha-1-antitrypsin deficiency).
  • Age ≥18 years and ≤80 years
  • Affiliated person or beneficiary of a social security regime
  • Written informed consent of the patient who agree to comply with the study protocol.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (20)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University hospital of Angers
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AngersFranceRecruiting
University hospital of Besançon
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BesançonFranceNot yet recruiting
Avicenne Hospital (Greater Paris University Hospitals)
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BobignyFranceNot yet recruiting
University Hospital of Dijon
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DijonFranceRecruiting
Departemental Hospital Center of Vendée
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La Roche-sur-YonFranceRecruiting
University Hospital of Grenoble
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La TroncheFranceActive, not recruiting
University Hospital of Lille
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LilleFranceActive, not recruiting
University Hospital of Limoges
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LimogesFranceActive, not recruiting
La Croix Rousse Hospital
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LyonFranceRecruiting
Edouard Herriot Hospital
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LyonFranceNot yet recruiting
Saint-Joseph Hospital
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MarseilleFranceNot yet recruiting
University Hospital of Montpellier
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MontpellierFranceRecruiting
University Hospital of Nantes
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NantesFranceActive, not recruiting
La Pitié Salpétrière Hospital (Greater Paris University Hospitals)
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ParisFranceNot yet recruiting
Saint-Antoine Hospital (Greater Paris University Hospitals)
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ParisFranceActive, not recruiting
Cochin Hospital
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ParisFranceNot yet recruiting
University Hospital of Bordeaux
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PessacFranceActive, not recruiting
University Hospital of Rennes
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RennesFranceActive, not recruiting
University Hospital of Tours
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ToursFranceActive, not recruiting
University Hospital of Nancy
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Vandœuvre-lès-NancyFranceNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.