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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02869698
Other study ID # 38RC09.012
Secondary ID
Status Completed
Phase N/A
First received August 4, 2016
Last updated October 25, 2017
Start date June 2009
Est. completion date September 2017

Study information

Verified date October 2017
Source University Hospital, Grenoble
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This prospective research aims to develop the use of Spectral Imaging in addition Dynamics of cortical electrical stimulation to identify major anatomical and functional networks in epileptic patients candidates for surgery and explored by stereoencephalography, to minimize risk of post-surgical cognitive deficits.


Description:

Cognitive deficits after epilepsy surgery are poorly known particularly because the tools used to evaluate them. In addition, the prevention of certain postoperative deficits, is extremely difficult because of the lack of robust markers to anticipate. The various examinations conventionally used for this purpose (neuropsychological testing, functional MRI and cortical stimulation) does indeed provide insufficient information or difficult to interpret, so the development of improved methods appears as an imperative in the field of the epilepsy surgery.

SID appears as such particularly adapted to the case of epileptic patients explored SEEG to provide individualized cognitive map millimeter thereof without requiring, for additional invasive act, or risk of inducing unintended crisis. In practice, this clinical research project should lead to the definition of several simple cognitive tasks which, together, could be achieved by each volunteer patient in two or three hours, and then analyzed in a similar time to provide fast, even the patient is still explored SEEG and even before cortical electrical stimulation, a list of brain regions involved in most major cognitive functions.


Recruitment information / eligibility

Status Completed
Enrollment 192
Est. completion date September 2017
Est. primary completion date May 2017
Accepts healthy volunteers No
Gender All
Age group 6 Years to 65 Years
Eligibility Inclusion Criteria:

- Drug-resistant partial epilepsy justifying a SEEG exploration

- Intellectual capacities compatible with the award of cognitive tasks

Exclusion Criteria:

- Pregnant or lactating women

- Patient deprived of liberty by a judicial or administrative

- Major patient subject to a measure of legal protection

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Spectral Dynamic Imaging

Device:
Hybride electrode

Macro electrode


Locations

Country Name City State
France University Hospital Grenoble Grenoble
France University Hospital Lyon Lyon

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Grenoble

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Functional brain mapping procedure using the EEG signal intracranial to minimize the risk of cognitive deficits associated with resection of the epileptogenic zone. 3 weeks
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