Evaluating non-invasive methods for predicting kidney failure in patients with liver complications

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the prognostic value of non-invasive assessments in patients experiencing acute-on-chronic liver failure (ACLF) and renal failure, both with and without the intervention of transjugular intrahepatic portosystemic shunt (TIPS). It involves a structured follow-up program where clinical and laboratory data are collected and analyzed to identify potential predictive markers. The study aims to enhance understanding of kidney failure progression in the context of liver disease using advanced imaging techniques and biomarkers.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* All patients with portal hypertension and kidney failure

Exclusion Criteria:

* no consent, no kidney failure, no portal hypertension

Where it's running

• University Hospital Bonn
  Bonn, Germany Recruiting

Study contacts

• Principal investigator: Michael Praktiknjo, MD — University Hospital, Bonn
• Study coordinator: Michael Praktiknjo, MD
• Email: michael.praktiknjo@ukbonn.de
• Phone: +49(0)228-287 15770

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.