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Recruiting NCT03644732

NCT03644732 Atlas of Human Cognition by SEEG (MAPCOG-SEEG)

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Clinical Trial Summary
NCT ID NCT03644732
Status Recruiting
Phase
Sponsor University Hospital, Grenoble
Condition Refractory Epilepsy
Study Type OBSERVATIONAL
Enrollment 200 participants
Start Date 2018-04-05
Primary Completion 2028-03

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 65 Years
Study Type OBSERVATIONAL
Interventions
SEEG Group

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 200 participants in total. It began in 2018-04-05 with a primary completion date of 2028-03.

⚠ 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

The main objective of MAPCOG\_SEEG is to create a database including brain recordings of cognition performed in clinical routine in patients during the pre-surgical SEEG assessment. This aims to be able to propose the first atlas of human cognition with a high temporal and spatial resolution.

Eligibility Criteria

Inclusion Criteria: * Drug-resistant focal epilepsy * Justified SEEG exploration in the context of presurgical assessment of epilepsy * Written non-opposition to study participation * Intellectual capacities compatible with the compliance in the cognitive tasks Exclusion Criteria: * Major Patient undergoing a legal protection measure or patient deprived of liberty as a result of a judicial or administrative decision * Impossibility of collecting information on exposure (recent arrival in France, foreign language, etc.) * Pregnant women (Contraindication to SEEG exploration)

Contact & Investigator

Central Contact

Philippe Kahane, MD/PhD

✉ pkahane@chu-grenoble.fr

📞 +33 476 765 488

Principal Investigator

Philippe Kahane, MD/PhD

PRINCIPAL INVESTIGATOR

University Hospital, Grenoble

Frequently Asked Questions

Who can join the NCT03644732 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Refractory Epilepsy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT03644732 currently recruiting?

Yes, NCT03644732 is actively recruiting participants. Contact the research team at pkahane@chu-grenoble.fr for enrollment information.

Where is the NCT03644732 trial being conducted?

This trial is being conducted at Grenoble, France, Nancy, France, Paris, France, Rennes, France.

Who is sponsoring the NCT03644732 clinical trial?

NCT03644732 is sponsored by University Hospital, Grenoble. The principal investigator is Philippe Kahane, MD/PhD at University Hospital, Grenoble. The trial plans to enroll 200 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