RecruitingNCT06855056

Validation of New Prognostic Biomarkers in Patients With Decompensated Cirrhosis

Validation of New Prognostic biomarkerRs in Patients With cirrhOsis diScharged After a hosPitalization Due to acutE deCompensation or acuTe-on-chronic Liver Failure


Sponsor

European Foundation for Study of Chronic Liver Failure

Enrollment

189 participants

Start Date

Mar 1, 2025

Study Type

OBSERVATIONAL

Conditions

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


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This study looks for new blood markers (biomarkers) that can predict which patients with advanced liver scarring (decompensated cirrhosis) are most likely to have serious complications or die, helping doctors identify who needs closer monitoring after leaving the hospital. **You may be eligible if:** - You are between 18 and 80 years old - You were hospitalized due to complications of advanced liver disease (such as fluid in the abdomen, confusion, bleeding, or infection) - You have recovered enough to be discharged within 48 hours **You may NOT be eligible if:** - You were admitted for a planned procedure or test (not for liver complications) - You have active cancer (except certain types of liver cancer or skin cancer) - You are HIV-positive (unless on treatment without symptoms) - You have a history of liver transplant or other organ transplant - You have had a procedure to re-route blood around the liver (TIPS or porto-caval shunt) - You have severe kidney, heart, or lung disease - You have severe psychiatric illness or are expected to have poor adherence to the study - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(9)

Hospital Beaujon

Clichy, France, France

University Hospital, Aachen

Aachen, Germany, Germany

Universitätsklinikum Münster

Münster, Germany, Germany

IRCCS Azienda Ospedaliero Universitaria di Bologna Policlinico di S.Orsola

Bologna, Italia, Italy

A.O.U. Città della Salute e della Scienza di Torino

Torino, Italy, Italy

Hospital Universitari Vall d'Hebron Research Institute

Barcelona, Spain, Spain

Hospital Clinic de Barcelona

Barcelona, Spain, Spain

Hospital Universitario Ramon y Cajal

Madrid, Spain, Spain

Royal Free Hospital

London, United Kingdom, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT06855056


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