Language Function in Patients With Brain Tumors

NCT ID: NCT00599703

Last Updated: 2009-07-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

7 participants

Study Classification

OBSERVATIONAL

Study Start Date

2005-05-31

Study Completion Date

2009-03-31

Brief Summary

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The purpose of this study is to use an imaging method called functional magnetic resonance imaging (fMRI) in patients who have a tumor near an area of the brain that is believed to control language. The fMRI is a new kind of imaging that uses a strong magnetic field to look at functioning brain tissue. This kind of imaging will be used to study the effect of the brain tumor on your speech.

Detailed Description

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Conditions

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Brain Cancer CNS Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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1

neurosurgical patients

fMRI Scan, pre- and post language evaluation

Intervention Type OTHER

All subjects will undergo functional MR imaging, pre- and post-surgical language evaluation, and electrocortical stimulation mapping. The brain tumor patients will undergo these procedures twice.

Interventions

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fMRI Scan, pre- and post language evaluation

All subjects will undergo functional MR imaging, pre- and post-surgical language evaluation, and electrocortical stimulation mapping. The brain tumor patients will undergo these procedures twice.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient in whom a tumor invades or is directly adjacent to the expected location of one of the language centers.
* At least 18 years of age
* English as first language

Exclusion Criteria

* Patients with high grade tumors
* History of significant psychiatric condition (e.g. schizophrenia, obsessive-compulsive disorder, significant dementia),
* History of the following neurological conditions: CVA, demyelinating conditions, cerebral palsy, Alzheimer's disease.
* History of significant claustrophobic reactions.
* Pregnancy
* Standard contraindications to MR examinations (e.g. implanted stimulator)
* Patients, who were treated prior to our first scan, will not be eligible to participate in this study
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Memorial Sloan Kettering Cancer Center

OTHER

Sponsor Role lead

Responsible Party

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Memorial Sloan-Kettering Cancer Center

Principal Investigators

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Andrei Holodny, MD

Role: PRINCIPAL_INVESTIGATOR

Memorial Sloan Kettering Cancer Center

Locations

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Memorial Sloan Kettering Cancer Center

New York, New York, United States

Site Status

Countries

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United States

Related Links

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http://www.mskcc.org

Memorial Sloan-Kettering Cancer Center

Other Identifiers

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05-043

Identifier Type: -

Identifier Source: org_study_id

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