Actively Recruiting
Feasibility of Transcranial Focused Ultrasound to Measure Brain Tumor
Led by University of Minnesota · Updated on 2025-10-02
15
Participants Needed
1
Research Sites
214 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Transcranial focused ultrasound (tFUS) offers a platform for non-invasive imaging and treatment of the brain and pathology of the brain -- allowing high resolution imaging in both spatial and temporal dimensions. Compared with the gold- standard for brain imaging, magnetic resonance imaging (MRI), ultrasound offers reduced contrast while providing improved sampling in time through a significantly more cost-effective approach. In addition, while MRI is used to guide invasive treatments, only ultrasound can offer treatments through three primary mechanisms: 1) neuromodulation, 2) blood brain barrier modulation, and thermal/mechanical ablation through high intensity focused ultrasound (HIFU). All three treatment options require targeting therapy through the skull, which remains a barrier to clinical translation. This proposal is to test the feasibility of acquiring noninvasive targeting imaging intraoperatively prior to clinically indicated cranial neurosurgery. By acquiring volumetric ultrasound images while coregistered to previously obtained stereotactic magnetic resonance imaging, the study will be able to compare the ability of tFUS to identify and focus on brain pathology.
CONDITIONS
Official Title
Feasibility of Transcranial Focused Ultrasound to Measure Brain Tumor
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Able to undergo informed consent
- Scheduled and present for brain surgery
- General Anesthesia planned
- Neuronavigation used for surgery
- Thin cut post-contrast imaging available for coregistration
- At least 18 years of age
You will not qualify if you...
- Awake craniotomy planned
- Unhealed wounds or infection of scalp
- Diseases and conditions that would increase the morbidity and mortality of craniotomy and tumor resection as judged by the principal investigator
- Pregnancy (also generally required for surgery)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Minnesota
Minneapolis, Minnesota, United States, 55414
Actively Recruiting
Research Team
D
David Darrow, MD
CONTACT
C
Crina Peterson
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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