Blood tests could predict infections in ICU patients
NCT ID NCT02638779
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study looked at how the immune system is weakened after septic shock, severe trauma, burns, or major surgery. Researchers took blood samples from 552 patients and healthy volunteers to measure immune function. The goal was to find better ways to predict and manage infections in critically ill patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could provide tools to predict and manage infections in critically ill patients.
- What could go wrong
- This is an observational study, not a treatment trial. It may not lead to direct patient benefits.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
552 people
The number who actually took part.
- Started
-
Dec 2015
- Finished
-
Jun 2018
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria for patients * Patient or next of kin having been informed of the conditions of the study and having signed the informed consent form * Patient hospitalized for : * Septic shock * Severe trauma (including severe burn) * Major surgery Inclusion criteria for healthy volunteers * Normal clinical examination * Signed informed consent form * Person with social security insurance Exclusion criteria for patients * Patient with severe neutropenia (neutrophil count \<0.5 g/l) * Patients receiving immunosuppressive therapy * Patients receiving corticosteroids (IV or Per os) * Use of therapeutic antibodies * Hematological disease under treatment, or treated within 5 years before inclusion * End of chemotherapy within the 6 months prior to inclusion * Patient with innate or acquired immune deficiency (for example severe combined immunodeficiency, HIV or AIDS, any stage) * Patients for whom a care limitation was pronounced at time of enrolment * Anticipated length of stay before discharge from the ICU is estimated at less than 48 hours * Participation in an intervention study * Extra-corporeal circulation in the month preceding inclusion in case of cardiac surgery * Pregnant or breastfeeding women * Patient with no social security insurance, with restricted liberty or under legal protection Exclusion criteria for healthy volunteers * Person with an infectious syndrome during the last 90 days * Extreme physical stress within the last week * Person having received within the last 90 days, a treatment based on * Antivirals * Antibiotics * Antiparasitics * Antifungics * Person having received within the last 15 days, a treatment based on non-steroidal anti-inflammatory drugs (NSAIDs) * Person having received within the last 24 months, a treatment based on * Immunosuppressive therapy * Corticosteroids (IV or Per os) * Therapeutic antibodies * Chemotherapy * History of : * innate or acquired immune deficiency * Hematological disease * Solid tumor * Severe chronic disease * Surgery or hospitalization within the last 2 years * Pregnancy within the last year * Participation to a phase I clinical assay during the last year * Pregnant or breastfeeding women * Person with restricted liberty or under legal protection
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Major surgery are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Service d'Anesthésie Réanimation - Hôpital Edouard Herriot
Lyon, 69437, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Bedside eye scans may reveal hidden blood flow problems in septic shock
- Can two blood markers catch sepsis before it turns deadly?
- Two cheap blood ratios put to the test as sepsis death predictors
- Can a bedside ultrasound predict which septic shock patients will stop breathing on their own?
- Can a computer model speed up sepsis blood tests?
- A routine calcium reading could reveal how sick a sepsis patient really is