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Study identifier: NCT06892457 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

PHArmacotherapy Assessed Using Neuroprobing With TransOsseal Magnetic Stimulation

Condition: Epilepsy  ·  Sponsor: Insel Gruppe AG, University Hospital Bern

PhaseN/A
Planned participants40
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Cecilia Friedrichs-Maeder, MD, MSc.  ·  +41 79 394 44 63  ·  cecilia.friedrichs-maeder@insel.ch

Maxime Baud, MD-Phd  ·  +41 79 385 96 90  ·  maxime.baud.neuro@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

University Hospital BernBern, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT06892457