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
- Diseases
- Fatty liver disease (MASLD/MASH)
- 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
Sites (20)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University hospital of Angers Coordinator of this site? Confirm its status | Angers | France | Recruiting |
| University hospital of Besançon Coordinator of this site? Confirm its status | Besançon | France | Not yet recruiting |
| Avicenne Hospital (Greater Paris University Hospitals) Coordinator of this site? Confirm its status | Bobigny | France | Not yet recruiting |
| University Hospital of Dijon Coordinator of this site? Confirm its status | Dijon | France | Recruiting |
| Departemental Hospital Center of Vendée Coordinator of this site? Confirm its status | La Roche-sur-Yon | France | Recruiting |
| University Hospital of Grenoble Coordinator of this site? Confirm its status | La Tronche | France | Active, not recruiting |
| University Hospital of Lille Coordinator of this site? Confirm its status | Lille | France | Active, not recruiting |
| University Hospital of Limoges Coordinator of this site? Confirm its status | Limoges | France | Active, not recruiting |
| La Croix Rousse Hospital Coordinator of this site? Confirm its status | Lyon | France | Recruiting |
| Edouard Herriot Hospital Coordinator of this site? Confirm its status | Lyon | France | Not yet recruiting |
| Saint-Joseph Hospital Coordinator of this site? Confirm its status | Marseille | France | Not yet recruiting |
| University Hospital of Montpellier Coordinator of this site? Confirm its status | Montpellier | France | Recruiting |
| University Hospital of Nantes Coordinator of this site? Confirm its status | Nantes | France | Active, not recruiting |
| La Pitié Salpétrière Hospital (Greater Paris University Hospitals) Coordinator of this site? Confirm its status | Paris | France | Not yet recruiting |
| Saint-Antoine Hospital (Greater Paris University Hospitals) Coordinator of this site? Confirm its status | Paris | France | Active, not recruiting |
| Cochin Hospital Coordinator of this site? Confirm its status | Paris | France | Not yet recruiting |
| University Hospital of Bordeaux Coordinator of this site? Confirm its status | Pessac | France | Active, not recruiting |
| University Hospital of Rennes Coordinator of this site? Confirm its status | Rennes | France | Active, not recruiting |
| University Hospital of Tours Coordinator of this site? Confirm its status | Tours | France | Active, not recruiting |
| University Hospital of Nancy Coordinator of this site? Confirm its status | Vandœuvre-lès-Nancy | France | Not yet recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.