Actively Recruiting

Age: 18Years +
All Genders
NCT04578301

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

Led by University Hospital, Bonn · Updated on 2022-05-18

200

Participants Needed

1

Research Sites

327 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female adult (≥18 years) patient
  • With or without liver cirrhosis diagnosed by histology or clinical, laboratory, and radiological signs
  • Or with non-cirrhotic portal hypertension
  • Non-pregnant, non-lactating females
  • Ability to understand study information and provide written informed consent
  • Cooperative and available for the entire study
  • Indication for surgical intervention
Not Eligible

You will not qualify if you...

  • Pregnant or lactating females
  • Patients having surgery for palliative cancer treatment
  • Patients with severe extra-hepatic diseases
  • HIV-positive patients
  • Patients with previous liver or other organ transplant
  • Patients with acute or subacute liver failure without cirrhosis
  • Patients who decline participation
  • Physician's denial due to inability to follow protocol

AI-Screening

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Trial Site Locations

Total: 1 location

1

University Hospital Bonn

Bonn, Germany

Actively Recruiting

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Research Team

M

Michael Praktiknjo, MD

CONTACT

J

Johannes Chang, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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