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Advanced Magnetic Resonance Imaging in Temporal Lobe Epilepsy

Conditions
Temporal Lobe Epilepsy
Registration Number
NCT03643471
Lead Sponsor
Assiut University
Brief Summary

We aim to o evaluate the role of conventional and advanced MRI sequences in diagnosis of idiopathic temporal lobe epilepsy including identification and lateralization of epileptogenic focus.

Detailed Description

Patients with history of partial seizures with or without secondary generalization attending at outpatient clinic or admitted at Neurology department of Assuit University Hospital will be included in the study MRI study will be done for each patient. MR imaging will be performed on a 1.5-T MR imaging unit (Siemens, Sembra medical system,German).

Prospectively completed data forms will be analyzed and compared. Statistical tests appropriate to the nature of the data will be used.

All patients will not be subjected to risk of any kind during this study. All patients' data will be confidentially kept. Approval of the ethical committee of Faculty of Medicine, Assiut University.

An informed consent will be taken from all patients included in this study. The research will be conducted only by scientifically qualified and trained personnel.

The procedures included in this study have been already used in hospital and centers in and outside Egypt

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
50
Inclusion Criteria
  • patients with history of partial seizures with or without secondary generalization attending at outpatient clinic or admitted at Neurology department of Assuit University Hospital will be included in the study based on the following criteria:

    • Clinical features consistent with seizures of temporal lobe origin.
    • Focal ictal temporal lobe patterns recorded with EEG.
    • No lesion detected by conventional MR imaging other than mesial temporal sclerosis.
Exclusion Criteria
  • Any general contraindication of MRI in some cases as presence of para magnetic substance as pacemakers or in patients with claustrophobia.
  • Subjects with age less than 12 year old.
  • Patients with any structural lesion other than mesial temporal sclerosis identified on MR brain imaging.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Calculating the sensitivity,specificity and accuracy of hippocampal volumetry , T2 relaxometry , MR spectroscopy and diffusion tensor imaging in identification and lataeralization of epileptogenic focusbaseline

* Quantification of hippocampal volumes bilaterally by mean of hippocampal volumetry

* Change in metabolites ratio at the affected hippocampus by mean of MR spectroscopy

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Assiut university hospital

🇪🇬

Assiut, Egypt

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