Motor Evoked Potential and Cortical Silent Period in Migraine

NCT ID: NCT07250464

Last Updated: 2025-11-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-12-01

Study Completion Date

2026-02-01

Brief Summary

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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.

Detailed Description

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Rationale and Background:

Migraine is a neurological disorder that significantly impairs individual quality of life and imposes substantial economic burdens on healthcare systems worldwide. Although its pathophysiology is not fully understood, recent research suggests that migraine is associated not only with vascular changes but also with alterations at neurological and cortical levels (Goadsby et al., 2017). Evidence increasingly indicates enhanced excitability and disrupted inhibitory mechanisms in central nervous system regions, including the motor cortex (Coppola et al., 2007).

Transcranial Magnetic Stimulation (TMS) is a non-invasive and reliable neurophysiological technique that stimulates the motor cortex and records muscle responses. Parameters obtained through TMS, such as Motor Evoked Potential (MEP) and Cortical Silent Period (CSP), are used to assess cortical excitability and inhibitory control, respectively (Chen et al., 1999). CSP is particularly useful for evaluating GABA-B-mediated inhibitory mechanisms. The hypothesis that migraine patients exhibit reduced cortical inhibition can be directly tested using CSP measurements.

Previous studies have reported shortened CSP durations and increased MEP amplitudes in migraine patients, suggesting cortical hyperexcitability (Brighina et al., 2002; Afra et al., 1998). However, these findings are inconsistent, and how they vary across migraine subtypes (with aura vs. without aura) remains unclear. Therefore, this study aims to characterize cortical physiological changes in migraine using objective and quantitative measures, filling gaps in the literature and contributing to clinical evaluations. Additionally, the relationship of these parameters with clinical features such as migraine type, duration, and attack frequency will be investigated to lay the groundwork for individualized neurophysiological profiling.

Primary and Secondary Objectives:

Primary Objective:

The primary objective of this study is to objectively evaluate inhibitory control in the motor cortex of migraine patients using non-invasive methods. Motor Evoked Potentials (MEP) and Cortical Silent Periods (CSP) obtained through TMS will be measured and compared between migraine patients and healthy controls. CSP duration, reflecting GABA-B-mediated inhibitory mechanisms, allows direct assessment of migraine's effect on cortical inhibition (Chen et al., 1999).

Secondary Objectives:

Motor Output Analysis: Electromyographic (EMG) signals will be analyzed using Peristimulus Time Histogram (PSTH) and Peristimulus Frequencygram (PSF) methods to assess the temporal pattern and frequency changes of motor unit responses following TMS. PSTH analyzes the timing of individual motor units after stimulation, while PSF provides a more precise view of post-stimulation frequency changes (Türker \& Powers, 2001). These analyses help reveal the spinal reflection of cortical stimulation and its effect on motor output.

Biomarker Potential: TMS-derived parameters such as CSP and MEP will be evaluated for their potential as biomarkers of migraine pathophysiology, contributing to the development of objective measures for future diagnosis and treatment.

Expected Benefits:

At the end of this study, it is expected to obtain objective data on motor cortical inhibitory capacity in migraine patients. TMS parameters, particularly CSP and MEP, can be used to understand the neurophysiological basis of migraine. The results may provide:

Improved understanding of cortical excitability and inhibition balance in migraine pathophysiology.

Foundational data for the development of objective diagnostic biomarkers for migraine.

Evidence of cortical dysfunction in migraine patients, supporting personalized treatment approaches.

A comprehensive understanding of motor output from cortical to spinal levels via electrophysiological analyses (PSTH/PSF).

All procedures are non-invasive and safe, providing a reproducible and ethical research approach.

Study Methods:

Participants:

The study will include right-handed individuals aged 18-45 years with a prior diagnosis of migraine according to the International Headache Society (IHS) criteria.

Data Collection:

The study will use non-invasive brain stimulation (TMS) along with surface electromyography (sEMG) and needle EMG. Measurements will be performed both at rest and during voluntary muscle contraction. TMS will be applied over the motor cortex, and muscle responses will be recorded simultaneously using sEMG electrodes. For detailed motor neuron analysis, single motor unit (SMU) recordings will also be obtained.

Needle EMG/SMU Recording:

SMU recordings will use sterile, Teflon-coated needles containing copper wires (approximately 70 μm diameter, 25G) inserted into the first dorsal interosseous (FDI) muscle. Needles will be partially retracted to maintain electrode stability, allowing single motor unit activity to be recorded even during movement.

TMS Application:

TMS will be performed using a Magstim 200\^2 Monophasic Stimulator (Magstim Ltd, UK) with a 70 mm figure-of-eight coil placed over the dominant hemisphere's primary motor cortex (M1) corresponding to the FDI muscle. Resting Motor Threshold (RMT) will be determined, followed by stimulation to elicit MEPs.

Surface EMG Recording:

sEMG signals will be obtained using Ag/AgCl electrodes placed over the FDI muscle. Signals will be amplified with a CED 1902 amplifier and digitized via CED 3601 Power 1401 DAC unit. MEP latencies and amplitudes, as well as CSP durations, will be calculated. Participants will maintain \~20% maximal voluntary contraction during measurements.

Data Analysis:

Data will be analyzed using IBM SPSS Statistics 26. Normality will be tested using Kolmogorov-Smirnov and Shapiro-Wilk tests. Parametric data will be analyzed using independent t-tests and ANOVA, while non-parametric data will be analyzed with Mann-Whitney U or Kruskal-Wallis tests. Correlations between clinical parameters (migraine duration, frequency, severity) and neurophysiological measures (MEP, CSP) will be assessed using Pearson or Spearman correlation coefficients, with significance set at p \< 0.05.

Conditions

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Migraine Healty Controls

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Two groups (migraine patients and healthy controls) are evaluated in parallel. Participants and the responsible investigators are blinded to group assignments to reduce bias. Only the staff performing TMS and EMG measurements are aware of group allocation.
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

SINGLE

Outcome Assessors
Participants and responsible investigators do not know group assignments. Only the technical staff performing TMS and EMG recordings are aware of group allocation.

Study Groups

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Migraine Patients

Adult participants aged 18-45 with a prior diagnosis of migraine according to IHS criteria.

Transcranial Magnetic Stimulation (TMS)

Surface Electromyography (sEMG)

Needle EMG / Single Motor Unit (SMU) Recording

Group Type EXPERIMENTAL

Transcranial Magnetic Stimulation (TMS)

Intervention Type OTHER

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)

Intervention Type DEVICE

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

Intervention Type OTHER

Sterile Teflon-coated needle electrodes inserted into the FDI muscle to record activity of individual motor units during TMS and voluntary contractions.

Healthy Controls

Age- and sex-matched adults without a history of migraine or neurological disorders.

They undergo the same sEMG and needle EMG/SMU procedures as the migraine group, but the TMS is sham.

Surface Electromyography (sEMG)

Needle EMG / Single Motor Unit (SMU) Recording

Transcranial Magnetic Stimulation (TMS) SHAM

Group Type SHAM_COMPARATOR

Surface Electromyography (sEMG)

Intervention Type DEVICE

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

Intervention Type OTHER

Sterile Teflon-coated needle electrodes inserted into the FDI muscle to record activity of individual motor units during TMS and voluntary contractions.

Interventions

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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.

Intervention Type OTHER

Surface Electromyography (sEMG)

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

Intervention Type DEVICE

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.

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Istanbul Gelisim University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Kemal Sıtkı Türker, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

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

Locations

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

Istanbul, Istanbul, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Central Contacts

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Murat Kara, MSc

Role: CONTACT

+905314708141

Kemal Sıtkı Türker, Prof. Dr.

Role: CONTACT

+905325987791

Facility Contacts

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Murat Kara, MSc

Role: primary

+905314708141

Kemal Sıtkı Türker, Prof. Dr.

Role: backup

+905325987791

References

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Haavik H, Niazi IK, Jochumsen M, Ugincius P, Sebik O, Yilmaz G, Navid MS, Ozyurt MG, Turker KS. Chiropractic spinal manipulation alters TMS induced I-wave excitability and shortens the cortical silent period. J Electromyogr Kinesiol. 2018 Oct;42:24-35. doi: 10.1016/j.jelekin.2018.06.010. Epub 2018 Jun 19.

Reference Type BACKGROUND
PMID: 29936314 (View on PubMed)

Ozyurt MG, Haavik H, Nedergaard RW, Topkara B, Senocak BS, Goztepe MB, Niazi IK, Turker KS. Transcranial magnetic stimulation induced early silent period and rebound activity re-examined. PLoS One. 2019 Dec 4;14(12):e0225535. doi: 10.1371/journal.pone.0225535. eCollection 2019.

Reference Type BACKGROUND
PMID: 31800618 (View on PubMed)

Todd G, Rogasch NC, Turker KS. Transcranial magnetic stimulation and peristimulus frequencygram. Clin Neurophysiol. 2012 May;123(5):1002-9. doi: 10.1016/j.clinph.2011.09.019. Epub 2011 Oct 22.

Reference Type BACKGROUND
PMID: 22019353 (View on PubMed)

Haavik, H., Özyurt, M. G., Niazi, I. K., Nedergaard, R. W., Topkara, B., Yilmaz, G., & Türker, K. S. (2018). Re-investigation on the nature and sign of transcranial magnetic stimulation-induced cortical silent period. In 11th Biennial Meeting of the International Motoneuron Society, IBS, 11-14 June 2018, Boulder, CO, USA (pp. 28-29). Article 46 https://motoneuron2018.org/wp-content/uploads/2018/05/IMS-Poster-Abstracts-2018.pdf

Reference Type BACKGROUND

Kahya MC, Yavuz SU, Turker KS. Cutaneous silent period in human FDI motor units. Exp Brain Res. 2010 Sep;205(4):455-63. doi: 10.1007/s00221-010-2380-6. Epub 2010 Aug 8.

Reference Type BACKGROUND
PMID: 20694723 (View on PubMed)

Provided Documents

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Document Type: Study Protocol

View Document

Document Type: Informed Consent Form

View Document

Related Links

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https://www.example.com/

No public protocol page available; contact [email protected] for study information.

Other Identifiers

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IGU-ENF-MK-1

Identifier Type: -

Identifier Source: org_study_id

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