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Clinical Trial Summary

This single-center prospective observational study aims at characterization of pathogenesis of ACLF. There will be three different cohorts investigated with the main endpoint mortality in these groups. 1. SAPIENT = Sepsis ACLF patients, to investigate the differences between ACLF and sepsis in cirrhosis 2. PROACT = Portal mediators as ACLF Targets, to assess portal venous biomarkers in patients receiving TIPS leading to ACLF and identify potential treatment targets 3. ELITE = prEdictors of beneficial LIver Tx in ACFL patiEnts, to assess in ACLF-patients receiving liver transplantation predictors of survival, which may improve selection of ACLF-patients for liver transplantation Secondary endpoints will be different in the three different cohorts and biological material will be collected for separate ancillary studies.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04975490
Study type Observational
Source Johann Wolfgang Goethe University Hospital
Contact Jonel Trebicka, MD, PhD
Phone +4963014256
Email jonel.trebicka@kgu.de
Status Recruiting
Phase
Start date December 1, 2020
Completion date December 31, 2025

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