Actively Recruiting

Age: 18Years +
All Genders
NCT06892457

PHArmacotherapy Assessed Using Neuroprobing With TransOsseal Magnetic Stimulation

Led by Insel Gruppe AG, University Hospital Bern · Updated on 2025-03-24

40

Participants Needed

1

Research Sites

258 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this observational study is to investigate how prescribed anti-seizure medications (ASMs) affect cortical excitability in adults with epilepsy. The main questions it aims to answer are: 1. Does the magnitude of transcranial magnetic stimulation (TMS)-evoked potentials (TEPs) measured with electroencephalography (EEG) change between OFF and ON medication states? 2. Do these changes in TEP amplitude persist over time? Researchers will compare each participant's measurements in the OFF state with those in the ON state to see if TEPs change following ASM (re)start. Participants will undergo one TMS-EEG session scheduled around their prescribed ASM (re)start and one 1-6 months later.

CONDITIONS

Official Title

PHArmacotherapy Assessed Using Neuroprobing With TransOsseal Magnetic Stimulation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older with epilepsy prescribed anti-seizure medication for clinical reasons
  • Written informed consent provided
Not Eligible

You will not qualify if you...

  • Electrical implants (e.g., neurostimulator or drug delivery system) or metallic implants in the head (excluding teeth)
  • Increased intracranial pressure
  • Uncontrolled psychiatric disorder
  • Use of any drugs or alcohol (nicotine allowed)
  • Pregnancy cannot be ruled out with sufficient certainty in female participants (pregnancy test required before TMS)
  • Inability to provide informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Bern

Bern, Switzerland, 3010

Actively Recruiting

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Research Team

C

Cecilia Friedrichs-Maeder, MD, MSc.

CONTACT

M

Maxime Baud, MD-Phd

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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