The objective of this multicentre study is to collect preoperative, intra operative, early, short, intermediate and mid-term(one years) on the related clinical complications and functional outcomes of market-approved Alcis products to demonstrate safety and performance of these devices in a real-world setting.
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Eligibility Criteria
Inclusion Criteria:
* To be included, patients must be:
* 18 months to 65 years
* Patient with drug-resistant and disabling focal epilepsy
* Informed and willing to sign an informed consent form approved by EC / For minors: if one of the parents cannot consent within the timeframe provided by the p…
Inclusion Criteria:
* To be included, patients must be:
* 18 months to 65 years
* Patient with drug-resistant and disabling focal epilepsy
* Informed and willing to sign an informed consent form approved by EC / For minors: if one of the parents cannot consent within the timeframe provided by the protocol, then only one parent's signature is required
* Affiliation to the social security or foreign regime recognized in France
* For prospective inclusion: Patient considered for SEEG exploration as part of pre-surgical assessment of epilepsy
* For ambispective inclusion:
* Must have undergone an SEEG exploration with one ALCIS device before the date of the initiation visit
* Follow-up visits (at least 12-month) must be prospective
* Must have complete information available for each completed visit (demographics, preoperative information, implantation information, device details) \*.
Exclusion Criteria:
* • Not able to comply with the study procedures based on the judgment of the assessor (e.g. cannot comprehend study questions, inability to keep scheduled assessment times)
* Any medical condition that could impact the study at investigator's discretion (e.g. allergy…)
* Pregnant women (contraindication to SEEG exploration)
* Adult subject to legal protection measure
* Skull thickness inferior at 2 mm
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