Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06105645

Contribution of Fast-ripples to the Improvement of the Neurosurgical Management of Drug-refractory Epilepsy

Led by University Hospital, Toulouse · Updated on 2025-09-22

440

Participants Needed

11

Research Sites

323 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Toulouse

Lead Sponsor

C

Centre de recherche Cerveau et Cognition (CERCO)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The main aim of this study is to evaluate the contribution of fast-ripples (FR) information on the neurosurgery management of patients with drug-refractory epilepsy investigated by Stereo-ElectroEncephaloGraphy (SEEG), as measured by freedom from disabling seizures one-year post-surgery. 220 patients (for whom 4-6 usual clinical macro-electrodes will be replaced by hybrid micro-macro electrodes and for whom fast-ripples will be assessed) distributed over 5 centres and 220 control patients(who will undergo an SEEG with the usual electrodes and for whom fast-ripples will not be assessed) distributed over 6 centres. This is a controlled, non-randomized, parallel plan, prospective, multicentre exploratory study.

CONDITIONS

Official Title

Contribution of Fast-ripples to the Improvement of the Neurosurgical Management of Drug-refractory Epilepsy

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient suffering from drug-resistant focal epilepsy (DRFE), as defined by the International League Against Epilepsy, undergoing SEEG selected by a multidisciplinary epilepsy meeting
  • Patient who has given written informed consent for study data collection
  • Patient covered by the French healthcare system
Not Eligible

You will not qualify if you...

  • Patients under juridical protection (authorship, curatorship, or safeguarding of justice)
  • Patient deprived of liberty by judicial or administrative decision
  • Patient with a cardiac defibrillator
  • Thermocoagulation planned on any potential hybrid electrode
  • Patient currently in exclusion period of another study
  • Patients not meeting criteria for SEEG

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 11 locations

1

CHU Amiens Picardie

Amiens, France

Actively Recruiting

2

University hospital of Bordeaux

Bordeaux, France, 33076

Actively Recruiting

3

University hospital of Grenoble Alpes

La Tronche, France, 38700

Actively Recruiting

4

APHP Hôpital Bicêtre

Le Kremlin-Bicêtre, France, 94270

Actively Recruiting

5

CHU de Lille

Lille, France

Actively Recruiting

6

Hospices Civils de Lyon

Lyon, France

Actively Recruiting

7

CHRU de Nancy

Nancy, France

Actively Recruiting

8

Fondation Adolphe de Rothschild

Paris, France, 75019

Not Yet Recruiting

9

CHU de Rennes

Rennes, France

Actively Recruiting

10

Hôpitaux universitaires de Strasbourg

Strasbourg, France

Actively Recruiting

11

University Hospital of Toulouse

Toulouse, France, 31059

Actively Recruiting

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Research Team

L

Luc VALTON, MD

CONTACT

Y

Yoan HERADES

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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