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Recruiting NCT06202976

NCT06202976 Mapping Epileptic Networks Using Multimodal Imaging

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Clinical Trial Summary
NCT ID NCT06202976
Status Recruiting
Phase
Sponsor Imagine Institute
Condition Epilepsy in Children
Study Type OBSERVATIONAL
Enrollment 75 participants
Start Date 2017-09-14
Primary Completion 2033-09-13

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age 18 Years
Study Type OBSERVATIONAL
Interventions
Secondary data collection

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 75 participants in total. It began in 2017-09-14 with a primary completion date of 2033-09-13.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Currently, mapping the epileptogenic zone is based on a comprehensive preoperative assessment involving clinical, imaging and electrophysiological examinations. To reduce the need for invasive stereoelectroencephalography (SEEG) explorations, electrophysiological and imaging methods have been developed, such as resting-state functional MRI (fMRI) coupled with electroencephalogram and arterial spin-labeling perfusion MRI (ASL-MRI). It has been published that these new methods enable precise delineation of the epileptogenic zone and better preparation for surgery. The aim is to determine whether, in children with focal lesional epilepsy, the combination of ASL-MRI-EEG and resting-state fMRI-EEG enables precise identification of the epileptogenic zone to be defined by SEEG, the current reference examination.

Eligibility Criteria

Inclusion Criteria: * Be under 18 years of age on the day of inclusion. * Present with one of the following forms of epilepsy: * refractory focal lesional epilepsy * rare non-lesional epilepsy * Present abnormalities (spikes) on the intercritical EEG * Have been selected by the "Epilepsy" multidisciplinary staff. * In the case of refractory lesional epilepsy, be required to perform an EEG-video recording using intracranial electrodes (SEEG) as part of the pre-surgical workup. * Be affiliated to a health insurance scheme. Exclusion Criteria: * Requiring general anesthesia for MRI * Require sedation specifically for research * Have generalized epilepsy * Be deprived of liberty or under guardianship.

Contact & Investigator

Central Contact

Nathalie Boddaert, Pr

✉ nathalie.boddaert@aphp.fr

📞 +33 (0)1 44 49 51 75

Frequently Asked Questions

Who can join the NCT06202976 clinical trial?

This trial is open to participants of all sexes, up to 18 Years, studying Epilepsy in Children. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06202976 currently recruiting?

Yes, NCT06202976 is actively recruiting participants. Contact the research team at nathalie.boddaert@aphp.fr for enrollment information.

Where is the NCT06202976 trial being conducted?

This trial is being conducted at Paris, France.

Who is sponsoring the NCT06202976 clinical trial?

NCT06202976 is sponsored by Imagine Institute. The trial plans to enroll 75 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology