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NCT07119957Recruiting

ProspEXPO : Study of the Associations Between Hepatocellular Carcinoma and Chemical and Psychosocial Environmental EXPOsome

ProspEXPO : PROSPective Study of the Associations Between Hepatocellular Carcinoma and Chemical and Psychosocial Environmental EXPOsome

Source: ClinicalTrials.gov · Last updated 10 Jun 2026

Brief summary (registry, in English)

The aim of the study is to build up a bio-collection of biological samples from patients with cirrhosis. Further work using this bio-collection will permit to describe the influence of different exposome factors (nutrition, physical activity, socio-demographic conditions, tobacco, alcohol, pollutants) on the occurrence of the main type of liver cancer (called HCC). Indeed, in the vast majority of cases, HCC develops within cirrhosis, and the factors that precipitate the progression of cirrhotic patients to HCC remain largely unknown.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
300 (estimated)
First submitted
9 Jul 2025
Start date
17 Dec 2025
Primary completion date
Dec 2028
Lead sponsor
University Hospital, Angers
NCT number
NCT07119957

What you commit to

  • Study type: Interventional
  • Planned participants: 300
  • From 17 Dec 2025 to the primary completion date, Dec 2028
  • 4 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, not your situation.

Who cannot take part

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

Prior treatment

  • Decompensation of cirrhosis in the two years prior to inclusion (ascites, hepatic encephalopathy, gastrointestinal variceal hemorrhage, liver failure, hepatorenal syndrome)

Other illness

  • Causes of chronic liver disease other than MASLD, ALD, or MetALD
  • For the "Control" group: history of hepatocellular carcinoma

Other

  • Pregnant, breast-feeding or parturient women
  • Persons deprived of liberty by judicial or administrative decision

Who the study is looking for

  • Presence of metabolic and/or alcoholic steatotic liver disease, as defined by the new nomenclature (MASLD, ALD, or mixed MetALD)
  • Liver biopsy performed (less than 2 months ago) or planned as part of treatment for diagnosis of cirrhosis ("Control" group without HCC) or diagnosis of HCC on cirrhosis ("Case" group)
  • Patient affiliated to or benefiting from a social security scheme
  • Patient having signed an informed consent to participate in the study (bio-collection)

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

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Angers University Hospital
Coordinator of this site? Confirm its status
AngersFranceRecruiting
Rennes University Hospital, Hepatogastroenteroly Department
Coordinator of this site? Confirm its status
RennesFranceNot yet recruiting
Centre Eugène Marquis (Oncology center)
Coordinator of this site? Confirm its status
RennesFranceNot yet recruiting
Tours University Hospital, HepatoGastroenterology Department
Coordinator of this site? Confirm its status
ToursFranceNot yet recruiting

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