Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06892457

PHArmacotherapy Assessed Using Neuroprobing With TransOsseal Magnetic Stimulation

Status
Recruiting
Phase
Study type
Observational
Enrollment
40 (estimated)
Sponsor
Insel Gruppe AG, University Hospital Bern · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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

Interventions

TypeNameDescription
OTHERTMS-EEGEvoked brain activity is measured with the help of TMS-EEG in epilepsy patients OFF and ON medication.

Timeline

Start date
2024-10-21
Primary completion
2029-10-01
Completion
2029-10-01
First posted
2025-03-24
Last updated
2025-03-24

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT06892457. Inclusion in this directory is not an endorsement.