SEP 8, 2026 · INTERVENTIONAL STUDY
Early Endotoxin Burden Reduction With oXiris in Septic Shock Patients Requiring CRRT
ClinicalTrials.gov
This is a single-center, uncontrolled pilot study with no comparator group and an estimated enrollment of only 13 participants, designed to assess feasibility and biological effect on a surrogate endpoint (endotoxin level) rather than clinical outcomes.
Reported
Planned enrollment13
Primary outcome measureChange from baseline in blood endotoxin lev…
Study duration (intervention)24 hours of CRRT with oXiris