Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05335187

Hybrid Micro-macro Electrodes in Patients With Epilepsy

Led by Pierre Mégevand · Updated on 2026-05-05

30

Participants Needed

2

Research Sites

230 weeks

Total Duration

On this page

Sponsors

P

Pierre Mégevand

Lead Sponsor

S

Swiss National Science Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of the MicroEPI study is to know whether it is possible to use safely a medical device (a micro-electrode) that allows recording the activity of neurons in the human brain. Patients who suffer from drug-resistant epilepsy and who are candidates to epilepsy surgery to alleviate their condition sometimes require the implantation of intracranial EEG electrodes for a few weeks, in order to determine as best as possible which region of the brain to operate on. In the MicroEPI study, some of these electrodes will also comprise micro-electrodes, allowing us to record the activity of the patients' neurons during their epileptic seizures.

CONDITIONS

Official Title

Hybrid Micro-macro Electrodes in Patients With Epilepsy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient 18 years old or older suffering from drug-resistant focal epilepsy.
  • Candidate for epilepsy surgery.
  • Requires evaluation with intracranial stereo-EEG electrodes.
  • Able and willing to provide informed consent.
Not Eligible

You will not qualify if you...

  • Any acute infection (e.g. fever, throat infection).
  • Skin or scalp infection over the implantation site.
  • Thin or fragile skull bones preventing safe electrode anchoring.
  • Increased risk of infections from medical conditions or immunosuppressant medication.
  • Increased risk of bleeding from medical conditions or antiplatelet/anticoagulant medication.
  • Severe medical diseases including cardiovascular, respiratory, renal, or hepatic disease.
  • Severe psychiatric disease or major psychological distress.
  • Women who are pregnant or breastfeeding during the study.
  • Patients with implanted stimulation devices such as pacemakers, defibrillators, or neurostimulators.

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Inselspital Bern

Bern, Canton of Bern, Switzerland, 3010

Actively Recruiting

2

Hôpitaux Universitaires de Genève

Geneva, CH, Switzerland, 1205

Actively Recruiting

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Research Team

P

Pierre Mégevand, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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Hybrid Micro-macro Electrodes in Patients With Epilepsy | DecenTrialz