About this trial
In order to better determine which therapy is best for patiënts which present with organ falure during the course of their stay in the intesive care unit (ICU) , one has to determine which underlying mechanism is causing this organ falure. We will determine levels of so called "biomarkers" for ferroptosis (a mechan ism of iron-related cell death) in the peripheral blood and biological fluids of criticaly ill patients admitted to the ICU with a catastrrophy (severe infection, trauma ...) . Why ? If it turns out that this ferroptosis plays a role in the ocurrence of organ failure in the critially ill, this will lead to new therapies in the future as drugs become more and more available which can influene this biochemical "pahway". of iron-relatd death.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Admitted to the ICU of UZA
Critically ill and predicted to be hospitalised in the ICU for > 48 hours (i.e. mostly patients admitted for sepsis, trauma, haemorrhagic shock, neurological catastrophe … which means at risk to develop mono-or multiple organ failure)
With arterial line in place (for blood sampling)
Disqualifiers
Refusal of consent by patient or closest relative
Postoperative patients after major surgery in whom prolonged ICU stay is not foreseen (i.e. elective cardiac surgery
Trial design
Single group
Treatments tested in this trial
Blood sampling
Diagnostic testBlood sampling: 3 first days of admision, 2 ml of plasma daily Urine, BALF, CSF sampling: 1 day during 3 first days of admission
Treatment groups
Trial outcomes
Primary outcomes
Number of patients with survival after 28 days.
Survival in and after ICU.
Secondary outcomes
Change from baseline concentration of Norepinephrine every day during ICU stay
Change in SOFA score during ICU stay
SOFA score, with a higher score for more severe organ failure
Sponsors and contacts
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University Hospital, Antwerp
Lead sponsor
Universiteit Antwerpen
Collaborator