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Clinical Trial Summary

This is a prospective, randomized, open-label, multicentre study involving European centers with experience in the management of PHLF to assess the impact of early liver support with MARS on survival in patients with post-hepatectomy liver failure (PHLF).


Clinical Trial Description

PHLF is a major risk factor for mortality in patients who underwent major hepatectomy. A specific treatment is yet not available. In a primary proof-of-concept study, it was shown that it is safe and feasible to use MARS in patients with PHLF early after hepatectomy. Survival was superior to a historical control group.

This study will include patients with early, primary PHLF (based on the 50:50 criteria) after major liver surgery. Patients will be randomized 1:1 to receive standard treatment alone or standard treatment + liver dialysis using the Molecular Adsorbent Recirculating System (MARS). Relevant outcome along with several physiological parameters will be assessed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03761238
Study type Interventional
Source Karolinska University Hospital
Contact Stefan Gilg, MD PhD
Phone 0702677722
Email stefan.gilg@ki.se
Status Not yet recruiting
Phase N/A
Start date March 15, 2019
Completion date September 15, 2022

See also
  Status Clinical Trial Phase
Withdrawn NCT05280990 - HepaRAS Trial: Changes in Hepatectomy Risk Assessment When Using Mebrofenin HIDA N/A
Recruiting NCT04692259 - May the Risk of PHLF be Predicted With Preoperative Liver Gadoxetate MRI N/A