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Advanced Magnetic Resonance Imaging in Temporal Lobe Epilepsy

A

Assiut University

Status

Unknown

Conditions

Temporal Lobe Epilepsy

Treatments

Device: MRI

Study type

Observational

Funder types

Other

Identifiers

NCT03643471
MRI in temporal lobe epilepsy

Details and patient eligibility

About

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.

Full 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

Enrollment

50 estimated patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

1

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Central trial contact

Osama Haris, doctorate; Radwa Anas, Master

Data sourced from clinicaltrials.gov

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