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Completed

NCT Number: NCT05002400

Evaluation of the PS100B for the Diagnostic of Stroke With Patients Out of Delay for Thrombolysis or Thrombectomy

Numerous patients are addressed to the Emergency Department for unspecific symptoms which can evoke a stroke, such as vertigo, isolated motor deficit, behavior disorder.

For these patients, when they arrive out of time for specific treatments such as thrombolysis and thrombectomy, the cerebral imagery is not an emergency, but necessary to confirm or invalidate the diagnostic of stroke.

If a biomarker could exclude the diagnostic of stroke, we could avoid an imagery for these patients.

PS100B is a biomarker whose blood level increases in case of stroke. It has already proven a prognostic value. Until now, it hasn't proven a diagnostic value because it take a few hours to increase in the blood.

It could have in prognostic value for patients who have the symptoms for more than 24 hours.

STROkE is a diagnostic, prospective, monocentric study, conducted at University Hospital Center of Poitiers (France).

The aim is to determine the value of PS100B to exclude the diagnostic of a stroke in case of evocative symptoms, for patients who are out of delay for a thrombolysis or a thrombectomy.

Patients eligible are the ones who present to the emergency department with symptoms evocative of stroke for more than 24 hours and less than 4 days. Patients included have a sample of blood withdrawn, in order to measure PS100B blood level.

The diagnostic of stroke is than confirmed or excluded by an adjudication comity, who are unaware of the result of PS100B blood level.

The diagnostic value of PS100B is determined with the help of a ROC curve.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHU Henri MONDOR, Créteil, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Diagnostic value of PS100B

    Time frame: 1 day

    Determine the best couple sensibility / specificity of the blood value of PS100B with the help of a Receive Operating Charasteristics (ROC) curve for patients who present with symptoms evocative of stroke since more than 24 hours and less than 4 days

Secondary outcomes

  1. Value of PS100B for ischemic strokes and hemorrhagic strokes

    Time frame: 1 day

    Comparison of the mean value of PS100B between patients with ischemic strokes and hemorrhagic strokes

  2. Value of PS100B and time delay since the beginning of the symptoms

    Time frame: 1 day

    Stratification of the value of PS100B with the delay of apparition of the symptoms and realization of the blood sample

  3. Prognostic value of PS100B

    Time frame: 28 days

    Comparison of the value of PS100B and the patient's outcomes 28 days after inclusion. The patient's outcome will be assessed as follow : hospitalization, death and self-rated health perception.

    The self-rated health perception will be assessed with the scale EuroQOL (EQ)-5D-5L. The scale EQ-5D-5L is composed of :

    • a score on 5 levels : from 1 to 3 (no problem) and 4 to 5 (with problems)
    • analogic scale from 0 to 100 (0 = worst health perception ; 100 = best health perception)

Sponsors and collaborators

Lead sponsor

Poitiers University Hospital

Other

Registry information

Important dates

Study start
2021
Primary completion
2025
Study completion
2025
First posted
Aug 12, 2021
Registry last updated
Jan 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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