EPI-CATCHER: Innovative MRI to Localize the Epileptic Zone

Sponsor
University Hospital, Grenoble (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06057233
Collaborator
Université Grenoble-Alpes (Other), Institut National de la Santé Et de la Recherche Médicale, France (Other)
40
56

Study Details

Study Description

Brief Summary

The goal of EPI-CATCHER is to outline the clinical potential of multiparametric quantitative MRI (mqMRI) and of GABA-edited magnetic resonance spectroscopy (GABA-MRS), combined with machine learning tools, as imaging biomarkers to localize and delineate the EZ.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: mqMRI and GABA-MRS

Detailed Description

After informed consent, patient candidate to resection surgery will undergo two extra MRI sessions before surgery: one for multiparametric quantitative MRI (mqMRI) and one for GABA-edited magnetic resonance spectroscopy (GABA-MRS) In parallel, a group of healthy volunteers will also undergo the two MRI sessions described above, to collect reference data.

Study Design

Study Type:
Observational
Anticipated Enrollment :
40 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Quantitative MRI and GABA Spectroscopy to Localize the Epileptic Zone
Anticipated Study Start Date :
Oct 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2028
Anticipated Study Completion Date :
Jun 1, 2028

Arms and Interventions

Arm Intervention/Treatment
Patients

mqMRI and GABA-MRS data will be collected in patients suffering from mesial temporal lobe epilepsy

Diagnostic Test: mqMRI and GABA-MRS
multiparametric quantitative MRI (mqMRI) and of GABA-edited magnetic resonance spectroscopy (GABA-MRS)

Volunteers

mqMRI and GABA-MRS data will be collected in healthy volunteers

Diagnostic Test: mqMRI and GABA-MRS
multiparametric quantitative MRI (mqMRI) and of GABA-edited magnetic resonance spectroscopy (GABA-MRS)

Outcome Measures

Primary Outcome Measures

  1. EZmri vs EZsdt [5 years]

    The correlation coefficient between the Dice similarity coefficient (= 2 * the Area of Overlap between EZMRI and EZsdt divided by the total number of pixels in EZMRI and EZsdt) and the reduction in seizure frequency (= seizure frequency one year after surgery / seizure frequency at inclusion).

Secondary Outcome Measures

  1. mqMRI : T1 (ms) [5 years]

    Compare, for each patient, the mqMRI parameter values measured in the EZsdt with the mean mqMRI parameter values obtained in the same region across the healthy volunteers

  2. mqMRI : T2 (ms) [5 years]

    Compare, for each patient, the mqMRI parameter values measured in the EZsdt with the mean mqMRI parameter values obtained in the same region across the healthy volunteers

  3. mqMRI : Mean Diffusivity (s/mm²) [5 years]

    Compare, for each patient, the mqMRI parameter values measured in the EZsdt with the mean mqMRI parameter values obtained in the same region across the healthy volunteers

  4. mqMRI : Cerebral Blood Volume (%) [5 years]

    Compare, for each patient, the mqMRI parameter values measured in the EZsdt with the mean mqMRI parameter values obtained in the same region across the healthy volunteers

  5. mqMRI : Blood-Brain Barrier Permeability (%) [5 years]

    Compare, for each patient, the mqMRI parameter values measured in the EZsdt with the mean mqMRI parameter values obtained in the same region across the healthy volunteers

  6. GABA [5 years]

    Compare, for each patient, the amplitude of GABA and other metabolites available using proton MRS (N-acetyl aspartate and N-acetyl-aspartyl-glutamate (NAA) Creatine and phosphocreatine (Cr), Choline (Cho), Myo-inositol, myo-inositol-monophosphate and glycine (mI), Glutamine (Gln), glutamate (Glu), Lipids (LipX), Lactate (Lac)) in the EZsdt with the mean values obtained in the same region across the healthy volunteers

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patient group

  • Patients aged 18-65 years,

  • Patients with drug-resistant focal epilepsy,

  • Patients with MTLE suspicion, with normal MRI or hippocampal sclerosis, and candidate for surgery,

  • Negative pregnancy test for child-bearing aged woman,

  • Obtained signed informed consent from patient

  • Reference group

  • Male or female, 18-65 years,

  • Obtained signed informed consent from participants,

  • Negative pregnancy test for child-bearing aged woman

Exclusion Criteria:
  • Patient group

  • Patient without social security system

  • Inability or unwillingness of the individual to provide written informed consent, according to national regulations.

  • Impossibility of collecting information on exposure (subjects recently arrived in France, foreign language, etc.),

  • Contraindication for MRI,

  • Contraindication for injection of MRI contrast agent (Gd-Chelate),

  • Evidence on neuroimaging (CT or MRI) of a brain lesion in the same hemisphere as the EZ (tumor, stroke, cerebral edema with midline shift and a clinically significant compression of ventricles, or subarachnoid hemorrhage, or intracerebral parenchymal hematoma (petechial small hemorrhages are NOT a non-inclusion criteria),

  • Severe leucoariosis

  • Pre-existing dementia

  • Pregnant, breastfeeding women

  • Reference group

  • Person who is participating in another therapeutic trial

  • Person with a psychiatric disorder, an epilepsy, or a brain lesion susceptible to impact the MRI readouts

  • Person without social security system,

  • Inability or unwillingness of the individual to provide written informed consent, according to national regulations,

  • Impossibility of collecting information on exposure (subjects recently arrived in France, foreign language, etc.),

  • Contraindication for MRI

  • Contraindication for injection of MRI contrast agent (Gd-Chelate)

  • Pregnant, breastfeeding woman.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University Hospital, Grenoble
  • Université Grenoble-Alpes
  • Institut National de la Santé Et de la Recherche Médicale, France

Investigators

  • Principal Investigator: Philippe Kahane, MD, PhD, Université Grenoble-Alpes

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University Hospital, Grenoble
ClinicalTrials.gov Identifier:
NCT06057233
Other Study ID Numbers:
  • 38RC22.0265_EPI-CATCHER
  • ANR-21-CE17-0031
  • 2022-A01949-34
First Posted:
Sep 28, 2023
Last Update Posted:
Oct 5, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Grenoble
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 5, 2023