High-field MR Imaging in Migraine, Visual Snow and Epilepsy

NCT05524493 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2025-10-08

No results posted yet for this study

Summary

In this project, the aim is to recruit patients with drug resistant epilepsy and those suffering from migraine. Interestingly, patients suffering from epilepsy are also more often reporting to suffer from migraine. The pathobiology is understudied, but it is believed that both etiologies results from brain networks changes. A clinical certified 7T Terra Siemens scanner will be employed to assess in all participants (including healthy controls) how the microstructure differs in disease specific areas. Patients will further be clinically assessed as well as undergo questionnaires.

Migraine is also a common comorbidity to visual snow syndrom and has been shown to impact similar brain regions. However, the pathophysiology is still understudied and a better understanding of the two diseases is needed.

Conditions

Interventions

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Structural MRI

We will examine migraine and epilepsy patients as well as healthy controls using conventional structural MRI in the brain and spinal cord including T1-, T2-, and T2\*-weighted sequences

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Quantitative MRI

We will examine migraine and epilepsy patients as well as healthy controls using quantitative MRI in the brain and spinal cord. This includes multi-parameter mapping (MPM) and quantitative susceptibility mapping (QSM).

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Diffusion MRI

We will examine migraine and epilepsy patients as well as healthy controls using diffusion MRI in both brain and spinal cord.

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fMRI

We will examine migraine and epilepsy patients as well as healthy controls using resting-state and task fMRI (including sensory stimulation using pain stimulus) in both brain and spinal cord.

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MR Spectroscopy

We will examine migraine and epilepsy patients as well as healthy controls using MR Spectroscopy in both brain and spinal cord.

Sponsors & Collaborators

  • Balgrist University Hospital

    collaborator OTHER
  • University of Zurich

    lead OTHER

Principal Investigators

  • Patrick Freund, Prof. Dr. med. Dr. rer. nat. · University of Zurich

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-03-01
Primary Completion
2026-06-30
Completion
2026-06-30

Countries

  • Switzerland

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05524493 on ClinicalTrials.gov