Actively Recruiting

Age: 18Years +
All Genders
ID04690972

Constitution of a Biological Collection to Establish Preclinical Translational Models for the Study of Tumors and Chronic Liver Diseases

Led by Institut National de la Santé Et de la Recherche Médicale, France · Updated on 2026-02-12

800

Participants Needed

1

Research Sites

449 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying chronic liver diseases and tumors, including non-alcoholic steatohepatitis (NASH), non-alcoholic fatty liver disease (NAFLD), cirrhosis, and hepatocellular carcinoma (HCC). These conditions can be caused by viral infections like hepatitis B, C, and D or lifestyle factors such as overeating and lack of exercise. The goal is to develop better understanding and new treatments by analyzing liver tissues and tumors at the single-cell level to identify therapeutic targets and improve patient outcomes. The study involves creating patient-derived preclinical models, such as spheroid cultures and mouse xenograft models, to test new treatment strategies. Blood samples and tissue biopsies are collected during surgeries, biopsies, or diagnostic tests. Researchers use advanced molecular techniques like single-cell RNA sequencing to examine tumor heterogeneity and the liver environment, aiming to discover new biomarkers and treatment predictors. Participants will undergo procedures as part of their care, including hepato-bilio-pancreatic surgery, biopsies, or locoregional treatments. Blood samples are taken during these procedures to support research. Researchers will monitor surgery outcomes over an average of eight years. By studying patient samples and clinical data, the team aims to improve personalized medicine approaches and identify new preventive and therapeutic targets for chronic liver diseases and liver cancer.

CONDITIONS

Brief Title

"Constitution of a Biological Collection to Establish Preclinical Translational Models for the Study of Tumors and Chronic Liver Diseases".

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with chronic liver disease (viral or non-viral)
  • Patients diagnosed with at least one liver nodule scheduled for biopsy
  • Patients planned for hepatobiliary surgery as part of care
  • Patients for whom locoregional treatment for hepatocellular carcinoma (HCC) is indicated
  • Patients able to understand study information and provide written informed consent
  • Patients affiliated with the French social security system
Not Eligible

You will not qualify if you...

  • Minor patients
  • Patients under legal protection or unable to provide consent
  • Patients in situations of social fragility
  • Pregnant or breastfeeding women
  • Patients who have not signed informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Variable, depending on care schedule

Participants undergo diagnostic procedures such as blood sampling as part of their routine care to help characterize their liver condition.

1 or more visits depending on diagnostic tests

Surgery and Immediate Post-operative Care

Duration - Up to hospital discharge

Participants who undergo hepato-bilio-pancreatic surgery as part of their routine care have blood samples taken during surgery and receive immediate post-operative monitoring.

1 surgical visit plus approximately 6 post-operative visits

Sample Collection

Duration - Single procedure visit

Participants scheduled for biopsy or locoregional treatment have additional biopsy samples and blood drawn to support research analyses.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 8 years

Participants with chronic liver disease are followed over time to monitor disease progression and support ongoing research.

Periodic visits as part of routine care

Trial Site Locations

Total: 1 location

1

PU-PH, Directeur de l'UMR_S1110 Unité Inserm d'affiliation : UMR_S1110

Strasbourg, France, 67000

Actively Recruiting

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Research Team

T

Thomas BAUMERT, DR

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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