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Blood test may speed up epilepsy diagnosis in ER

NCT ID NCT07527754

Diagnosis Sponsor: Assistance Publique - Hôpitaux de Paris Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether measuring a protein called S100B in the blood can help emergency doctors quickly tell if a person's fainting spell was caused by epilepsy or something else, like a heart problem. About 100 adults who come to the ER after losing consciousness will give an extra blood sample. Their final diagnosis will be checked three months later to see how accurate the S100B test is.

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

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Apr 2026

An estimate. Start dates often move.

Expected to finish

Jul 2027

An estimate. End dates often move.

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

The study population will consist of adult patients presenting to the Emergency Department of Henri Mondor University Hospital during the inclusion period for an episode of transient loss of consciousness. Eligible patients will be screened consecutively and included if they meet all predefined inclusion criteria and none of the 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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * • Adult ≥ 18 years old * Presentation to the Emergency Department of Henri Mondor University Hospital * History of loss of consciousness * Undergoing a blood test as part of Emergency Department care * Covered by social security * Has agreed to participate in the study Exclusion Criteria: * Symptoms occurring more than 12 hours ago * History of head trauma without brain imaging performed * History of head trauma with intracranial bleeding confirmed on brain imaging * Refusal to participate in the study * Pregnant and/or breastfeeding women * Individuals unable to provide consent, particularly due to cognitive impairment * Individuals under legal protection: * Placed under guardianship * Deprived of liberty (incarcerated or hospitalized without consent)

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Conditions

The condition(s) this trial relates to.

Adams-Stokes syndrome epilepsy

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Cryptogenic epilepsy Epilepsy

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Hôpital Henri Mondor

    Créteil, Île-de-France Region, 94000, France

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