About this trial
Prospective, observational study to define precipitants and predictors of development of Acute-on-Chronic Liver Failure (ACLF) after surgical interventions, allowing to develop a risk stratification for elective procedures in cirrhotic patients. As well as identifying molecular mechanisms of post-interventional ACLF and thus preparing the ground for development of new therapeutic approaches.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Male or female adult (≥18 years) patient
With or without liver cirrhosis (diagnosed either histologically or by a combination of clinical, laboratory and radiological signs)
Or Non-cirrhotic portal hypertension
Non-pregnant, non-lactating females
Disqualifiers
Pregnant or lactating females
Patients undergoing surgery as form of palliative cancer therapy
Presence or history of severe extra-hepatic diseases
HIV-positive patients
Trial population
Patients with and without liver cirrhosis and/or portal hypertension undergoing elective or emergency surgical intervention.
Trial design
Cohort
Prospective
Treatments tested in this trial
No Intervention
Other interventionNo Intervention
Treatment groups
Trial outcomes
Primary outcomes
Episodes of Acute-on-Chronic Liver Failure (ACLF)
Development of ACLF after surgery
Secondary outcomes
1-year mortality
Death after surgery
Episodes of Acute Decompensation
Acute hepatic Decompensation after Surgery
Other outcomes
Intestinal Microbiota
Intestinal Microbiota will be assessed in stool samples.
Sponsors and contacts
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