Stratifying Critically Ill Patients for Novel Ferroptosis or Pyroptosis Intervention Strategies
Recruiting
N/A
Interventional Study
Sepsis
Trauma Related Injuries
Subarachnoid Haemorrhage (SAH)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Diagnostic
- Participants needed
- 600 (estimated)
- Sponsor
- University Hospital, Antwerp · Other
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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 cr…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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 arter…
Contacts