Actively Recruiting

Phase Not Applicable
Age: 3Years +
All Genders
ID06059157

Epileptogenic Network Visualization Using Advanced MRI in Drug-Resistant Epilepsy

Led by Cliniques universitaires Saint-Luc- Université Catholique de Louvain · Updated on 2024-03-18

80

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to improve the non-invasive identification of epileptogenic networks in patients with drug-resistant epilepsy. It compares the standard stereo-EEG method with advanced MRI techniques including resting-state functional MRI and microstructural analysis of white matter. The study focuses on the accuracy of identifying epileptogenic networks and how MRI sequences affect patient selection and target identification for surgery. Participants already selected for stereo-EEG will undergo an additional MRI session lasting about one hour, including 3D T1, resting-state fMRI, and multishell diffusion sequences. The MRI data will be processed to map epileptogenic networks and analyze connections between brain regions. Patients undergoing therapeutic epilepsy surgery will have a follow-up MRI three months after the operation to assess changes in these networks. During the study, participants will have MRI scans before and, if applicable, after surgery. Researchers will analyze MRI data with advanced algorithms to evaluate network identification, quantification, and regulation post-surgery. The main outcomes include network identification accuracy after about three years, prognosis one year after surgery, and the added value of radiological analysis in standard epilepsy evaluation approximately one year after phase three begins. Safety and feasibility will be monitored throughout the participation period.

CONDITIONS

Brief Title

Epileptogenic Network Visualisation With Advanced MRI

Who Can Participate

Age: 3Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient suffering from drug-resistant epilepsy
  • Patient already selected for stereo-EEG implantation as part of their epileptic networks
  • Age 3 years or older
Not Eligible

You will not qualify if you...

  • Patient excluded from stereo-EEG (including pregnant women, children too young for the procedure, or those unable to undergo the procedure)
  • Contraindication for MRI

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Up to 3 years

Participants undergo advanced MRI scans including resting-state functional MRI, diffusion with advanced post-processing, and myelin mapping to identify epileptogenic networks.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Based on clinical care

Participants who receive curative surgery (resection or disconnection) undergo surgical treatment.

Post-operative Follow-up

Duration - 3 months after surgery

Participants who had surgery undergo a follow-up MRI 3 months after the procedure to evaluate changes in epileptogenic networks.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Cliniques Universitaires St-Luc

Brussels, Belgium, 1200

Actively Recruiting

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Research Team

R

Riëm El Tahry, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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