High-resolution Multi-parametric Magnetic Resonance Imaging for Focal Epilepsy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorChinese University of Hong Kong

About this trial

Patients with focal epilepsy often have diagnostic difficulties as their culprit for seizures are difficult to be picked up using conventional imaging. The current study is to investigate the utility of advanced MRI sequences on detection of subtle lesions accountable for focal epilepsy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Consecutive patients with drug-resistant focal epilepsy fulfilling the following criteria -

Clinical seminology compatible with focal epilepsy.

Electroencephalography pointing towards a specific site for focal epilepsy.

Positive ictal brain scintigraphy with SPECT-CT correlation. AND 2. Previous MRI (at least one study with protocol tailored for epilepsy) which did not reveal accountable focal lesion.

Disqualifiers

Patients who are contraindicated to magnetic resonance imaging (such as due to underlying MRI incompatible metallic implants)

Patients who cannot cooperate for MRI scanning.

Patients show are unable to provide informed consent.

Trial design

Design model

Single group

Treatments tested in this trial

  • Magnetic Resonance Imaging

    Diagnostic test

    Subjects will undergo MRI scanning in our 3T machine with dedicated high resolution sequences (including 2D T1-weighted inversion recovery sequences, 3D FLAIR MRI whole brain, 3D T1-weighted Sagittal MPRAGE; plus other sequences for the clinical purpose of pre-operative planning as per consensus with referring doctor)

Treatment groups

66 Participants
are divided into 1 treatment group
Group A: Study subjectsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Accuracy of high resolution MRI in diagnosis

the sensitivity and specificity of the baseline MRI (bMRI) and the high-resolution MRI (hrMRI) studies, based on the standard of surgical findings on patients who underwent either intracranial EEG or surgical resection

Time frame
At the time of MRI scanning, typically 1 day

Secondary outcomes

Other outcomes

Sponsors and contacts

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