Blood test may spare some stroke patients unnecessary brain scans
NCT ID NCT05002400
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a blood test measuring PS100B levels could help rule out stroke in patients with symptoms lasting more than 24 hours but less than 4 days. Researchers enrolled 179 patients at a French hospital. If the test proves accurate, it might reduce the need for emergency brain imaging in some cases.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- PS100B blood test
- What this could lead to
- If successful, this blood test could help doctors quickly rule out stroke in some patients, reducing the need for emergency brain scans.
- What could go wrong
- This is a small, early study (179 patients) looking at a biomarker that takes hours to rise, so it may not be reliable enough for routine use. The test is not yet proven to replace standard imaging.
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.
- Participants
-
179 people
The number who actually took part.
- Started
-
Sep 2021
- Finished
-
Dec 2025
- 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.
Who is studied
All patients presenting at the Emergency Department of the University Hospital Center of Poitiers for symptoms evocative of stroke for more then 24 hours and less then 4 days, that fit the inclusion and exclusion criteria
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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: * Patients presenting at the Emergency Department of the University Hospital Center of Poitiers for the following symptoms, which last since more then 24 hours et less then 4 days : * sensitive or motor deficit of one or several limbs * facial paralysis * impairment of speech * dysarthria * vertigo * impairment of vision * oculomotor disorder * diplopia * free patient, without guardianship or curatorship, or subordination * patient not objecting to research Exclusion Criteria: * head trauma that occured less then 15 days ago * known cerebral mass or melanoma * refusal to participate in research * patient benefiting from enhanced protection, namely: minors, persons deprived of their liberty by a judicial or administrative decision, adults under legal protection * pregnant and/or breastfeeding women
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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
-
C.H.U. de Poitiers
Poitiers, 86000, France
-
CHU Henri MONDOR
Créteil, 94000, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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