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WithdrawnNCT02795338Updated Sep 3, 2024

Multi-modality Localization of Eloquent Brain Function

An observational study in Brain Neoplasms, sponsored by University of Nebraska. Withdrawn. Open to participants aged 19 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-09-03.

Sponsored by University of Nebraska · Observational

Why this study was withdrawn
Project did not receive funding and was never started
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
0
Ages
19 Years and older
Sex
All
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Study summary

Accurate identification of areas of eloquent brain function is vital to surgical decision making and to preservation of independence as patients with brain tumors who are higher functioning have better survival outcomes. Eloquent brain is defined as a region controlling language, motor, or sensory function such that without its proper input, a person would be left with significant neurologic deficits. Imaging technology has evolved to provide multiple non-invasive modalities for pre-operative testing of eloquent brain function. Studies have shown that these non-invasive mapping modalities provide useful information, however, the information provided inconsistently predicts distribution of eloquent function.

Direct electrical stimulation (DES) at surgery allows assessment of eloquent function directly from the brain surface (invasive) and is considered the gold standard in brain mapping. Therefore, in order to determine the true clinical applicability of the non-invasive mapping technologies, this study proposes to assess the predictive value of functional MRI (fMRI) and magnetoencephalography (MEG) for sensorimotor and language functions by comparing results to DES and determine whether fMRI or MEG provides the most consistent and accurate information. The rationale for the proposed research is that understanding the reliability of our current technology will allow us to perform safer surgeries and to preserve neurologic function.

Read the detailed description

It is unknown whether imaging technologies have broad applications in brain mapping due to limited knowledge of the value of the results. Accurate identification of areas of eloquent brain function is vital to surgical decision making and to preservation of independence as patients with brain tumors who are higher functioning have better survival outcomes. Imaging technology has evolved to provide multiple non-invasive modalities for pre-operative testing of eloquent brain function and include functional MRI (fMRI) and magnetoencephalography (MEG). Eloquent brain is defined as a region controlling language, motor, or sensory function such that without its proper input, a person would be left with significant neurologic deficits. Studies conducted have shown that these non-invasive mapping modalities provide useful information, however, the information provided inconsistently predicts distribution of eloquent function.

Direct electrical stimulation (DES) at the time of surgery allows assessment of eloquent function directly from the brain surface (invasive) and is considered the gold standard in brain mapping. Therefore, in order to determine the true clinical applicability of the non-invasive mapping technologies, this study proposes to: (1) assess the predictive value of fMRI and MEG for sensorimotor and language functions by comparing their results to DES and (2) determine whether fMRI or MEG provides the most consistent and accurate information. These aims will be accomplished by by co-registering all mapping data (invasive and non-invasive) in a modifiable 3D rendering. In this way, the DES to fMRI and MEG can be evaluated as well as fMRI to MEG compared. The rationale for the proposed research is that understanding the reliability of our current technology will allow for safer surgeries and preservation of neurologic function. The expected outcomes for the work proposed in Aims 1 and 2 are identification of a predictive value for fMRI and MEG and determination if one modality should be utilized over the other pre-operatively for the most accurate information. The results of this study are expected to have an important positive impact because identification of accurate pre-operative non-invasive mapping modalities will allow tailored testing and possibly lead to negation of the need for intra-operative mapping in certain cases. It will also enhance patient outcomes by improving patient safety. Furthermore, it will serve as the basis for a multi-institutional mapping data bank.

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Conditions studied

  • Brain Neoplasms

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In context

Brain Neoplasms

1,960 studies on the registry are indexed under Brain Neoplasms; 515 are open to participants now.

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Lead sponsor

University of Nebraska is the lead sponsor of 473 studies on the registry; 66 are open to participants now.

Of its 75 completed or terminated interventional studies of FDA-regulated products, 46 (61%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

We propose enrolling 80 patients with brain tumors in or near eloquent brain regions who are appropriate candidates for surgery.

Inclusion criteria

  • informed consent
  • age equal to or greater than 19 years
  • gender: male and female included
  • brain tumor in or near an eloquent area of the brain that requires surgery
  • benign or malignant intra-axial brain tumor
  • primary or secondary intra-axial brain tumor
  • appropriate body habitus for operating room positioning and airway protection for awake mapping
  • appropriate mental status and capacity to participate with invasive or non-invasive mapping

Exclusion criteria

Exclusion Criteria:

  • any contraindication to MRI (i.e. implanted devices)
  • inappropriate body habitus for safe positioning or airway protection
  • no capacity to understand the study the study or consent to it
  • significant disability precluding successful mapping
  • positive pregnancy test in females
  • end stage renal disease or severe renal dysfunction
  • sleep apnea or any obstructive airway disease
  • severe anxiety disorder
  • metabolic encephalopathy
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
0 participants (actual)
Target follow-up
6 Months
Patient registry
Yes

Interventions

  • Procedurebrain mapping

    pre-operative and intra-operative brain mapping to identify eloquent areas

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What researchers measure

Primary outcomes

  1. Location in the brain of the fMRI activations relative to intra-operative brain mapping

    Assess the predictive value of fMRI for language and sensorimotor function by evaluating the location in the brain where the activity was found. The pre-operative locations will be compared to the intra-operative locations which are considered the gold standard. If the fMRI activations indicate the same gyrus/gyri as the intra-operative mapping, it is considered accurate. This is accomplished with special techniques integrating multiple data time points and types.

    Time frame: 5 years

  2. Location in the brain of the MEG activations relative to intra-operative brain mapping

    Assess the predictive value of MEG for language and sensorimotor function by evaluating the location in the brain where the activity was found. The pre-operative locations will be compared to the intra-operative locations which are considered the gold standard. If the MEG activations indicate the same gyrus/gyri as the intra-operative mapping, it is considered accurate. This is accomplished with special techniques integrating multiple data time points and types.

    Time frame: 5 years

  3. Accuracy of fMRI and MEG in pre-operative brain mapping

    Assess which mapping method provides the most consistent and accurate information in pre-operative mapping for language and sensorimotor function. Determination of the testing method that most often identifies the correct anatomic location of the eloquent function as dictated by the findings from outcomes 1 and 2.

    Time frame: 5 years

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 3, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02795338
Lead sponsor
University of Nebraska
Responsible party
Sponsor
First posted
Jun 10, 2016
Start date
Feb 27, 2018
Primary completion
Feb 27, 2018
Completion
Feb 27, 2018
Last update
Sep 3, 2024

Study contacts

Michele R Aizenberg Ansari, MD
principal investigator · University of Nebraska

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.

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