RecruitingNot Applicable

Validation of New Prognostic Biomarkers in Patients With Decompensated Cirrhosis

France, Germany, Italy189 participantsStarted 2025-03-01

Plain-language summary

The study aims to test the effectiveness of new biomarkers (measurable molecules in our body) in predicting the health outcome of patients with liver cirrhosis discharged from the hospital after a serious complication of the disease

Who can participate

Age range18 Years – 80 Years

SexALL

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Inclusion criteria

✓. Age between 18 and 80 years.
✓. Patients with decompensated cirrhosis admitted to hospital due to AD according to the EASL-CLIF criteria (rapid onset of ascites, hepatic encephalopathy, portal hypertensive- related gastrointestinal bleeding, bacterial infection, or any combination of these), including those who presented ACLF during hospitalization.
✓. Recovery from AD and expected to be discharged within the next 48 hours.

Exclusion criteria

✕. Admission for planned diagnostic or therapeutic procedures
✕. Active malignancy (except for hepatocellular carcinoma within the Milan criteria or nonmelanocytic skin cancer)
✕. Antiviral treatment for hepatitis C, B and delta initiated in the last 6 months or planned to be initiated in the following 6 months.
✕. HIV positive (except undergoing treatment and who do not exhibit clinical manifestations of AIDS).
✕. Ongoing alcohol use disorder with an expected low adherence to prescriptions as judged by physician
✕. Previous liver or other organ transplantation
✕. Patients with TIPS or other surgical porto-caval shunts
✕. Chronic organic renal failure stage IV and V or estimated Glomerular Filtration Rate \<20 ml/min according to the MDRD equations

What they're measuring

To test the prognostic accuracy of novel biomarkers identified within the DECISION project.

Timeframe: Until September 30th 2025

Trial details

NCT IDNCT06855056

SponsorEuropean Foundation for Study of Chronic Liver Failure

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2026-03-30

Contact for this trial

Anna Bosch

+34 93 227 14 03 anna.bosch@efclif.com

View on ClinicalTrials.gov More Liver Cirrhosis trials