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Clinical Trials in Germany / NCT04578301
Recruiting Observational

Predicting Acute-on-Chronic Liver Failure After Surgical Intervention in Chronic Liver Disease

NCT04578301 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2020-09-22
Last updated
2022-05-18

Condition(s) studied

Liver CirrhosisPortal HypertensionSurgeryAcute-On-Chronic Liver FailureNon-Cirrhotic Portal Hypertension

Investigational drug(s) / intervention(s)

No Intervention

No Intervention: No Intervention

Study summary

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 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 * Ability to understand the patient information and to personally sign and date the informed consent to participate in the study * The patient is co-operative and available for the entire study * Provided written informed consent * Indication for surgical intervention Exclusion Criteria: * Pregnant or lactating females * Patients undergoing surgery as form of palliative cancer therapy * Presence or history of severe extra-hepatic diseases * HIV-positive patients * Previous liver or other transplantation * Patients with acute or subacute liver failure without underlying cirrhosis * Patients who decline to participate * Physician´s denial (e.g. the investigator considers that the patient will not follow the protocol scheduled)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Hospital Bonn Bonn Germany Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04578301 on ClinicalTrials.gov ↗ ← All trials in Germany