Status:

RECRUITING

Enhanced MRI Imaging in Healthy Participants and Participants With Epilepsy

Lead Sponsor:

University of Alberta

Collaborating Sponsors:

Canadian Institutes of Health Research (CIHR)

Conditions:

Epilepsy, Temporal Lobe

Eligibility:

All Genders

18-64 years

Phase:

PHASE2

Brief Summary

Temporal lobe epilepsy (TLE) is a common type of epilepsy and one of the most likely to not be controlled by medication. For patients who do not respond to medication, surgery can result in a cure of ...

Detailed Description

Hippocampal sclerosis is the most common pathological finding in temporal lobe epilepsy. While CA1 and CA4 subregions are typically affected, considerable variability in the involvement of the differ...

Eligibility Criteria

Inclusion

  • Healthy controls aged 18-64.
  • Patients with temporal lobe epilepsy aged 18-64 and hippocampal sclerosis demonstrated on clinical MRI scan

Exclusion

  • Non-English speaking participants will be excluded as we cannot provide translation services.
  • Inability to provide informed consent.
  • Contraindications to MRI Age \< 17 years / \>65 years
  • Weight \> 127.5kg (which is the maximum weight of which a single 510mg vial of Ferumoxytol would accommodate a 4mg/kg dose).
  • Women of childbearing capacity with a positive pregnancy test
  • Women who are actively breast feeding
  • Contraindication of Ferumoxytol -known hypersensitivity to Feraheme or any of its components -History of allergic reaction to any intravenous iron product

Key Trial Info

Start Date :

May 1 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

September 1 2029

Estimated Enrollment :

50 Patients enrolled

Trial Details

Trial ID

NCT06483061

Start Date

May 1 2025

End Date

September 1 2029

Last Update

May 6 2025

Active Locations (1)

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1

Peter S. Allen MRI Unit

Edmonton, Alberta, Canada, T6G 2R3