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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02577757
Other study ID # CHU-Promoteur 2012-04
Secondary ID
Status Recruiting
Phase N/A
First received September 18, 2015
Last updated October 13, 2015
Start date November 2012
Est. completion date May 2016

Study information

Verified date October 2015
Source University Hospital, Angers
Contact ARAM TER MINASSIAN, physician
Phone +33.2.41.35.52.31
Email ArTerMinassian@chu-angers.fr
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

Proceed to an analysis of sensitivity and specificity results of the fMRI language network obtained in two ways: by providing a conventional language test and independent component analysis. These two methods will be compared to the reference method what the cortical intraoperative mapping.


Description:

Patients with brain tumors including malignant gliomas located in eloquent areas have long been considered inoperable because of median survival and predictable postoperative sequelae. The improved prognosis with chemoradiotherapy and surgical resection as complete as possible questioned this attitude. The goal is to operate those patients without additional disabilities. The cortical electrostimulation intraoperative mapping in awake surgery can meet the eloquent areas. Identifying with fMRI these same areas to better specify in advance the way initially and shortened the time to awake exploratory surgery which improves patient comfort. However anxiety induced by the review in a pre-operative setting, a debutante aphasia often make problematic the realization of a formal language test. The analysis in the low frequency of spontaneous oscillations of large neuronal networks can help isolate network of language at rest without particular language test at the group analysis. This methodology, however, needs to be validated at the individual level before it can be applied to pathology.

Proceed to an analysis of sensitivity and specificity results of the fMRI language network obtained in two ways: by providing a conventional language test and independent component analysis. These two methods will be compared to the reference method what the cortical intraoperative mapping.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date May 2016
Est. primary completion date May 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 7 Years and older
Eligibility Inclusion Criteria:

- Persons major and minor.

- Having given their written consent, or whose parents have given their written consent for minors.

- Affiliated with the social security system

- All patients eligible adults in awake surgery

- Affiliated with the social security system

- patient given their written consent

Exclusion Criteria

- Contraindications to MRI

- Pregnant or breastfeeding women

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Device:
MRI
MRI

Locations

Country Name City State
France CHU Angers Angers

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary MRI data obtained by comparing a formal language test to data obtained by a session of rest independent component analyzed in patients and volunteers 1 hour No
See also
  Status Clinical Trial Phase
Completed NCT03148470 - Impact of Theta Burst Stimulation Over the Left DLPFC on Language Switching N/A