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Clinical Trials/NCT02783391
NCT02783391UnknownNot Applicable

Pre and Per-operative Electrophysiological Cartography of Speech Area With Cortical Electrode Matrices

University Hospital, Grenoble2 sites in 1 country15 target enrollmentStarted: September 1, 2015Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
15
Locations
2
Primary Endpoint
electrophysiological recording
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

New method for speech area cartography in patient individual cortical anatomy in view of improving functional area limit preservation during surgery.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients needing cortectomy
  • •Male or female aged over 18 years
  • •Registered in the French social security scheme
  • •Signed informed consent

Exclusion Criteria

  • •All categories of protected persons

Outcomes

Primary Outcomes

electrophysiological recording

Time Frame: 2 hours

Electrophysiological recording of brain Speech Area, using Cortical Electrode Matrices, in order to improve functional area limit preservation during surgery

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University Hospital, Grenoble
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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