Antibodies Causing Epilepsy Syndromes: The ACES Study.

NCT ID: NCT02802475

Last Updated: 2022-07-28

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

582 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-12-31

Study Completion Date

2020-12-31

Brief Summary

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The Antibodies Causing Epilepsy Syndromes (ACES) Study is a observational cohort study focusing on detection of auto-immune epilepsy in patients with epilepsy of unknown origin.

Detailed Description

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Recently new treatable causes of epilepsy have been identified. These disorders are caused by a disruption of the balance in the brain caused by inflammation. This inflammatory reaction is caused by an autologous reaction of the immune system to specific brain proteins. The body produces antibodies to specific parts of the brain. These disorders can lead to epilepsy, memory dysfunction and psychiatric problems. Recognition is necessary for good treatment. Mostly anti-epileptic drugs are insufficient. These diseases can be treated with immune-modulating therapy. The ACES Study will focus on determining the frequencies of known antibodies and finding new, currently unknown, antibodies, causing epilepsy. Therefore patients will be investigated with epilepsy of unknown origin. To find new antibodies sera of patients with epilepsy will be added to brain sections of rats and to cultivated neuronal cells to look for a reaction. If new antibodies will be detected clinical features will be mapped of the patients. Also effects of antibodies on brain cells will be determined. Discovery of new antibodies can provide new treatment options for these patients. Also it will enable to discover more about the pathologic mechanisms of epilepsy.

Conditions

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Auto-immune Encephalitis Epilepsy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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acquired chronic, focal, epilepsy

patients ≥18 years of age, with acquired chronic epilepsy of unknown origin

vena punction

Intervention Type BIOLOGICAL

new onset epilepsy

patients ≥18 years of age, with new onset status epilepticus or new onset seizures with suspicion of limbic encephalitis

vena punction

Intervention Type BIOLOGICAL

Interventions

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vena punction

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Age of 18 and older.
* Status epilepticus or new onset seizures with signs of limbic encephalitis (clinical picture, MRI (FLAIR abnormalities), EEG abnormalities or CSF findings (CSF pleocytosis, increased IgG index, oligoclonal bands), or:
* Patients with acquired chronic focal epilepsy with an unknown cause.

Exclusion Criteria

* Children
* Epilepsy with known cause
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Nationaal Epilepsie Fonds

UNKNOWN

Sponsor Role collaborator

Erasmus Medical Center

OTHER

Sponsor Role lead

Responsible Party

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M.J. Titulaer

MD. PhD.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Maarten J Titulaer, MD,PhD

Role: PRINCIPAL_INVESTIGATOR

Erasmus Medical Center

Locations

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Epilepsiecentrum Kempenhaeghe

Heemstede, , Netherlands

Site Status

Stichting Epilepsie Instelling Nederland (SEIN)

Heemstede, , Netherlands

Site Status

Academic Hospital Maastricht

Maastricht, , Netherlands

Site Status

Erasmus Medisch Centrum

Rotterdam, , Netherlands

Site Status

Maasstad Hospital

Rotterdam, , Netherlands

Site Status

Haga Hospital

The Hague, , Netherlands

Site Status

St. Elisabeth Hospital

Tilburg, , Netherlands

Site Status

UMCU

Utrecht, , Netherlands

Site Status

Countries

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Netherlands

Other Identifiers

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MEC 2014-463

Identifier Type: -

Identifier Source: org_study_id

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