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Completed
NCT06855056
Validation of New Prognostic Biomarkers in Patients With Decompensated Cirrhosis
Conditions: Liver Cirrhosis, Decompensated Cirrhosis of Liver
Sex: All
Ages: 18 Years – 80 Years
Healthy volunteers: No
Enrollment: 189
Sponsor: European Foundation for Study of Chronic Liver Failure
Location: Hospital Beaujon Clichy
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 Criteria
Inclusion Criteria:
1. Age between 18 and 80 years.
2. 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.
3. Recovery from AD and expected to be discharged within the next 48 hours.
Exclusion Criteria:
1. Admission for planned diagnostic or therapeutic procedures
2. Active malignancy (except for hepatocellular carcinoma within the Milan criteria or nonmelanocytic skin cancer)
3. Antiviral treatment for hepatitis C, B and delta initiated in the last 6 months or planned to be initiated in the following 6 months.
4. HIV positive (except undergoing treatment and who do not exhibit clinical manifestations of AIDS).
5. Ongoing alcohol use disorder with an expected low adherence to prescriptions as judged by physician
6. Previous liver or other organ transplantation
7. Patients with TIPS or other surgical porto-caval shunts
8. Chronic organic renal failure stage IV and V or estimated Glomerular Filtration Rate \
Source: ClinicalTrials.gov (NCT06855056). StuddyBuddy aggregates publicly available trial information.