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Multimodal Imaging in Pre-surgical Evaluation of Epilepsy

Contribution of Multimodal Imaging (MRI, PET, MEG) in Pre-surgical Evaluation of Drug-resistant Focal Epilepsy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01735032
Acronym
EPIMAGE
Enrollment
140
Registered
2012-11-28
Start date
2012-10-31
Completion date
2016-05-31
Last updated
2012-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Partial Epilepsy

Keywords

focal epilepsy, pre-surgical evaluation, multimodal imaging, SEEG

Brief summary

Epilepsy is the most common chronic neurological disorder in the world, affecting more than 50 million people worldwide. Approximately 35% of patients with epilepsy are refractory to all available antiepileptic drugs. Drug-resistant epilepsies are often partial or focal. Patients with drug-resistant focal epilepsy suffer from an increased risk of death, primarily due to seizure-related fatalities, in comparison with the general population. The only therapeutic option for this form of epilepsy is the surgical removal of the region of the brain responsible for seizures, called the epileptogenic zone (EZ). This requires the precise localization of the EZ based on a comprehensive pre-surgical evaluation of patients. Today the gold standard for localizing the EZ and validating a non-invasive technique for localization of the EZ remains intracerebral stereo-EEG (stereo-electroencephalography or SEEG) recordings of spontaneous seizures. The implementation strategy of the intracerebral depth electrodes is guided by clinical and neuroimaging data, including anatomical Magnetic Resonance Imaging (MRI), Positron Emission Tomography (PET) with FDG (fluoro-Deoxy-Glucose) and MagnetoEncephaloGraphy (MEG). Although the contribution of each technique in the pre-surgical localization of the EZ has already been shown, no wide-scale study has examined the cumulative contribution of these three techniques.

Detailed description

The purpose of this study is (i) to evaluate rigorously the diagnostic value of multimodal imaging for non-invasive localization of the EZ and (ii) to better target the indications for intracerebral recordings (SEEG).

Interventions

None listed

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Patient with drug-resistant focal epilepsy * Candidates for pre-surgical evaluation including FDG PET, MRI, MEG and SEEG recordings. * Age 18-65 years * EEG-confirmed focal epilepsy for \>2 years * Signed informed consent form.

Exclusion criteria

* Age \<18 years and \>65 years * Contraindication to the MRI * Pregnant woman * Head size incompatible with MEG recordings * Adult subject to legal protection measure.

Design outcomes

Primary

MeasureTime frameDescription
Localizing value of MEG, FDG-PET and MRI for the determination of the Epileptogenic Zone defined by SEEG recordings180 daysPathological volumes defined by multimodal imaging (MEG, FDG-PET and MRI) will be compared to the topography of the EZ defined by SEEG recordings. For each patient, we will sum the total number of intracerebral depth electrodes included in the EZ. Then, for each functional volume obtained from multimodal data fusion, we will count the total number of electrodes in the latter (Vol elec\_tot) and the number of electrodes included in the EZ (Vol elec\_ze).

Secondary

MeasureTime frameDescription
sensitivity and specificity180 daysFor each functional volume, two parameters will be defined: sensitivity and specificity. These parameters will be calculated as follows: sensitivity = (Vol elec\_ze) / (Pat elec\_ze) and specificity = (Vol elec\_ze) / (Vol elec\_tot).

Countries

France

Contacts

Primary ContactJulien Jung, Dr.
julien.jung@chu-lyon.fr0033 472 117 833

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026