Trials / Completed
CompletedNCT03426943
Endotoxins and Cytokines Removal During Continuous Hemofiltration With oXiris™
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 39 (actual)
- Sponsor
- Hospices Civils de Lyon · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Sepsis is a major cause of death in Intensive Care Units and therefore finding new therapies to improve survival rates and limit morbidity is a major goal. Over the past decades, blood purification has been proposed as an adjuvant therapy for sepsis. The goal of blood purification is to restore the immune homeostasis and efficiency through the removal of bacterial products including endotoxins, broad-spectrum cytokines and other inflammatory mediators. Indeed, the large and overwhelmed release of these mediators in the early phase of sepsis may induce multiple organ failure syndrome. In 2017, different techniques are proposed for blood purification. Among them, the highly adsorptive membrane, oXiris™, seems promising. This membrane can be used in case of Acute Kidney Injury associated with sepsis and exhibits enhanced blood purification capacities. Previous studies on animals have already proven that this membrane can remove broad-spectrum cytokines but also endotoxins from the blood. This ability to remove endotoxins is particularly interesting since endotoxins are believed to be the trigger of the immune cascade at the initiation of sepsis. The lack of clinical evidence is the main limit to a wider use of this membrane. Therefore, the aim of the present clinical trial is to characterize the blood purification properties of the membrane in a human clinical setting. The oXiris™ membrane is specifically designed to improve the adsorptive capacities of the polyacrylonitrile-based AN69 membrane. Its extremely rich coating of polyethyleneimine (PEI) gives the membrane the ability to bind and remove not only cytokines but also endotoxins due to the positive charges of PEI at the surface of the membrane. The tested hypothesis is that the oXiris™ filter allows for a greater endotoxin and cytokine removal compared to a standard polysulfone ("PrismafleX HF1400") filter in patients with septic shock.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | Arterial blood sampling | All patients will have arterial blood sampling to assess pre-filter and post-filter plasma endotoxin mass and activity and plasma cytokine levels |
| BIOLOGICAL | Ultrafiltrate sampling | All patients will have ultrafiltrate sampling to assess cytokine levels |
| DEVICE | CVVH using oXiris™ filter | Patients included in the experimental arm will have renal replacement therapy by performing CVVH using oXiris™ filter |
| DEVICE | CVVH using PrismafleX HF1400 filter | Patients included in the experimental arm will have renal replacement therapy by performing CVVH using PrismafleX HF1400 filter |
Timeline
- Start date
- 2018-12-21
- Primary completion
- 2022-06-03
- Completion
- 2022-06-03
- First posted
- 2018-02-08
- Last updated
- 2023-12-05
Locations
8 sites across 1 country: France
Source: ClinicalTrials.gov record NCT03426943. Inclusion in this directory is not an endorsement.