Is Protein S100B a Predictor of First-to-chronic Seizure Conversion in Adults?
NCT ID: NCT02424123
Last Updated: 2023-12-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
37 participants
OBSERVATIONAL
2016-10-11
2020-07-30
Brief Summary
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The main objective of this study is to evaluate the association between the absolute (ng/ml) serum S100B levels (measured at time of the first seizure) and the experience, or not, of seizure recurrence within one year of follow-up.
Detailed Description
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A) Prognostic capacity of serum S100B levels to predict seizure recurrence. B) Association between the variation (%) of serum S100B levels between first seizure episode and scheduled follow-up (D14-D28) and seizure recurrence.
C) Correlation of S100B with IL-1b, IL-6, NSE serum levels at the same time points.
D) Association of serology data with: a) EEG profile (normal/abnormal); b) recurrence of seizures (Y/N).
E) Comparison of S100B serum levels in lesional vs non-lesional patients. F) Establishment of a bio-bank (serum and cells).
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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The study population
The study population is composed of patients between 18 and 60 years of age, of both sexes, recruited during consultations for a first epileptic seizure at the emergency department of Nîmes and Marseille Hospitals (CHRU).
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* The patient must have given his informed and signed consent.
* The patient must be insured or beneficiary of a health insurance plan.
* The patient is at least (≥) 18 years old and less than (\<) 60 years old.
* The patient has experienced a first generalized, epileptic seizure (patients with partial onset and secondary generalization can also be included).
* The seizure has occurred less than 24 hours ago.
Exclusion Criteria
* Within the past three months, the patient has participated in another study that may interfere with the results or conclusions of this study.
* The patient is in an exclusion period determined by a previous study.
* The patient is under judicial protection.
* The patient refuses to sign the consent.
* It is impossible to correctly inform the patient.
* The patient is pregnant or breast-feeding (MRI contraindicated).
* Patient has a previous abnormal brain imaging (MRI).
* Patient has abnormal biological tests for toxicology (alcohol, cocaine and cannabis tests), blood ionogram (hyponatremia \<130mM), liver enzymes (\>5N), inflammatory syndrome (elevated C-reactive protein).
18 Years
59 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de Nīmes
OTHER
Responsible Party
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Principal Investigators
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Nicola Marchi, MD
Role: STUDY_DIRECTOR
Institut de Génomique Fonctionnelle, CNRS, Montpellier
Locations
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APHM - Hôpital Nord
Marseille, , France
CHRU de Nîmes - Hôpital Universitaire Carémeau
Nîmes, , France
Countries
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Other Identifiers
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2015-A00157-42
Identifier Type: OTHER
Identifier Source: secondary_id
LOCAL/2014/ET-02
Identifier Type: -
Identifier Source: org_study_id