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Clinical Trials in Turkey / NCT07250464
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Motor Evoked Potential and Cortical Silent Period in Migraine

NCT07250464 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-12-01
Last updated
2025-11-28

Condition(s) studied

MigraineHealty Controls

Investigational drug(s) / intervention(s)

Transcranial Magnetic Stimulation (TMS)Surface Electromyography (sEMG)Needle EMG / Single Motor Unit (SMU) Recording

Transcranial Magnetic Stimulation (TMS): Non-invasive brain stimulation applied to the primary motor cortex to elicit motor evoked potentials (MEP) and cortical silent periods (CSP). 70 mm figure-of-eight coil used with Magstim 200² Monophasic Stimulator.

Surface Electromyography (sEMG): Bipolar Ag/AgCl electrodes placed over the first dorsal interosseous (FDI) muscle to record muscle responses to TMS.

Needle EMG / Single Motor Unit (SMU) Recording: Sterile Teflon-coated needle electrodes inserted into the FDI muscle to record activity of individual motor units during TMS and voluntary contractions.

Study summary

The primary objective of this study is to assess the level of inhibitory control in the motor cortex of migraine patients using objective and non-invasive methods. To this end, Motor Evoked Potential (MEP) and Cortical Silence Period (CSP) parameters obtained using Transcranial Magnetic Stimulation (TMS) will be measured and comparisons will be made between migraine patients and healthy controls. Since CSP duration is used specifically in the evaluation of GABA-B-mediated inhibitory mechanisms, it has the potential to directly measure the effect of migraine on cortical inhibition.

Eligibility

Sex
ALL
Min age
18 Years
Max age
45 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Age 18-45 years. * Right-handed individuals. * Migraine patients: diagnosed according to International Headache Society (IHS) criteria. * Healthy controls: no history of migraine or other neurological disorders. * Able and willing to provide informed consent. Exclusion Criteria: * History of epilepsy or other seizure disorders. * Presence of metal implants, pacemakers, or other contraindications to TMS. * Pregnancy or breastfeeding. * History of significant neurological or psychiatric disorders. * Use of medications that significantly alter cortical excitability (e.g., antiepileptics, benzodiazepines) in the last 2 weeks. * Any musculoskeletal condition preventing safe participation in EMG/TMS procedures.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Istanbul Gelisim University, Faculty of Dentistry, Translational Dentistry Research Laboratory Istanbul Istanbul

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07250464 on ClinicalTrials.gov ↗ ← All trials in Turkey