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Early Endotoxin Burden Reduction With oXiris in Septic Shock Patients Requiring CRRT

StatusRecruiting
PhaseNot applicable
Started2026-08-01
View on ClinicalTrials.gov ↗
The goal of this clinical trial is to learn whether continuous renal replacement therapy (CRRT) using the oXiris filter can lower the amount of endotoxin in the blood of adults with septic shock who need CRRT. Septic shock is a life-threatening condition caused by infection and severe organ dysfunction. CRRT is a form of continuous blood purification used to support the kidneys and manage fluid and waste products. The oXiris filter is designed to provide CRRT while also removing endotoxin and inflammatory substances from the blood. The main questions this study aims to answer are: Does 24 hours of CRRT with the oXiris filter lower blood endotoxin levels compared with levels before treatment? What changes occur in inflammation, organ function, and the need for medicines that raise blood pressure? What medical problems or treatment-related complications occur during the study? This is a single-center study with no comparison group. About 13 participants will take part, and all participants will receive CRRT with the oXiris filter for a planned period of 24 hours. Other treatments for septic shock, including treatment for infection, fluids, medicines to support blood pressure, and other organ support, will be provided according to the hospital's usual care. Researchers will: Collect blood samples before and after the 24-hour oXiris treatment to measure endotoxin and markers of inflammation. Record blood pressure, blood lactate, circulation, organ function, use of blood pressure medicines, and CRRT treatment information. Continue selected blood tests and clinical assessments during the first 7 days Record any medical problems, including serious medical problems, during the study. Check whether participants are alive at 28 days and 90 days after enrollment The study may help researchers better understand the biological effects and safety of the oXiris filter and provide information for larger future studies.
Trial Details
NCT Number NCT07807410
Lead Sponsor Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Conditions Septic Shock, Acute Kidney Injury
Enrollment 13 participants
Start Date 2026-08-01
Primary Completion 2027-05-01 (estimated)
Study Completion 2027-08-01 (estimated)
Updated on ClinicalTrials.gov 2026-09-08