Early Severe Illness TrAnslational BioLogy InformaticS in Humans

Recruiting Observational Study
Sepsis ARDS Critical Illness Neurocognitive Dysfunction Shock, Septic Ventilator Associated Pneumonia Immune Suppression Inflammation SIRS
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
1,000 (estimated)
Sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Other
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About This Trial
Advanced stages of the response to life-threatening infection, severe trauma, or other physiological insults often lead to exhaustion of the homeostatic mechanisms that sustain normal blood pressure and oxygenation. These syndromic presentations often meet the diagnostic criteria of sepsis and/or the acute respiratory distress syndrome (ARDS), the two most common syndromes encountered in the inten…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age ≥18 years old * ≤48h since ICU admission * ICU admission within 72h of presentation to the emergency department (ER) * Clinical critical illness suspected on the basis of any one of the following: 1. Altered mental status (GCS\<15) 2. Cardiovascular collapse (presence…
Contacts

Aleks Leligdowicz, MD PhD

519-661-2111

aleligdo@uwo.ca

CONTACT