Clotting clues: simple blood test eyed to catch sepsis before it turns deadly
NCT ID NCT07073456
First seen Sep 21, 2026 · Last updated Sep 21, 2026
Summary
Researchers want to know whether a bedside device that measures how blood clots can predict which patients with an infection will develop sepsis. The study enrolls 147 adults arriving at an emergency department with a suspected infection. Everyone gives blood for the clotting monitor and standard lab tests, with daily clotting readings for three days if they are admitted. The goal is to see whether any clotting measurement differs between patients who go on to develop sepsis within 72 hours and those who do not.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Viscoelastic Coagulation Monitor (VCM) blood test
- What this could lead to
- If it works, emergency doctors could use a quick bedside clotting test to flag which infected patients are sliding toward sepsis, so treatment starts sooner.
- What could go wrong
- This is an early, single-hospital observational study of 147 people, so it can only show a link between clotting readings and sepsis, not prove the test saves lives. Results may not hold in other hospitals or patient groups.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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147 people
The number who actually took part.
- Started
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Oct 2024
- Finished
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Oct 2025
- Lead sponsor
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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.
Who is studied
Patients, presenting to the Emergency Department of the General Hospital of Attikon, who meet all inclusion criteria and who do not meet any exclusion criterion will be enrolled in the study.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Adults male or female (age 18 years or more) * Suspicion of infection, defined according to medical judgment Exclusion Criteria: * Age less than 18 years * Denial for consent * Intake of any anti-coagulant medication the last one month * Intake of any anti-platelet medication the last one month * Intake of any biological disease modifying anti-rheumatic medication the last one month * Medical history of inflammatory bowel disease or pulmonary hypertension * Any medical history of hemophilia or congenital coagulation disorders * Any known solid tumor or hematologic malignancy irrespective the stage and treatment * Known infection by the hepatitis viruses B and C * Known infection by the human immunodeficiency virus * Pregnancy or lactation
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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
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4th Department of Internal Medicine, "Attikon" University Hospital, National and Kapodistrian University of Athens, Medical School
Chaïdári, Attica, 12462, Greece
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Emergency Medicine Department, Attikon University Hospital, NKUA
Chaïdári, 12462, Greece
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