EASEE4YOU: Neurostimulation with EASEE® for Adolescents with Epilepsy Aged 12–17 Years

The study in adolescents aged 12 to 17 further expands the evidence base on the safety and efficacy of the EASEE® System in drug-resistant focal epilepsy.

Unmet Need

Many adolescents with focal epilepsy fail to achieve adequate seizure control despite medication.

Innovative Treatment Approach

The EASEE® System uses transcranial focal cortex stimulation and is being studied in adolescents aged 12 to 17 for the first time.

Clinical Evidence

The study aims to provide important data on safety and efficacy and expand the evidence base for EASEE®.


The Study at a Glance

  • Indication: Drug-resistant focal epilepsy
  • Population: 35 adolescents aged 12 – 17
  • Intervention: EASEE® System
  • Study Design: International, multi-center, prospective study
  • Objective: Evaluation of the safety and efficacy of the treatment

Procedure

Inclusion

Patients who meet the study’s inclusion criteria

Baseline

Two month prospective baseline recording

Implantation

Implantation of the EASEE® Systems

Activation

Stimulation activated four weeks after implantation

Follow-up

Regular study visits

Study End

Three years after implantation

More Information on the EASEE4YOU Study

For further details on the study design, inclusion criteria, and study centers, please see the official study registry entry.

Clinical Evidence behind EASEE4YOU

Prof. Dr. med. Steffen Syrbe

Head of Pediatric Epileptology at Heidelberg University Hospital

Prof. Dr. med. Volker Arnd Coenen

Medical Director of the Department of Stereotactic and Functional Neurosurgery at Freiburg University Hospital


Interested in EASEE4YOU?

Our study team is happy to answer any questions you may have about EASEE4YOU.

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