Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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)
Duration - Based on clinical care
Participants who receive curative surgery (resection or disconnection) undergo surgical treatment.
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
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
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here