The purpose of this study is to evaluate the safety of BBB disruption using transcranial MRI-guided focused ultrasound in conjunction with an intravenous ultrasound contrast agent to increase the accumulation of doxorubicin in brain tumours and the adjacent brain using the ExAblate Transcranial system (220 kHz). Data will be collected to establish the basic safety of this type of treatment as the basis for later studies to evaluate its clinical efficacy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
MR Guided Focused Ultrasound
Sunnybrook Health Sciences Centre
Toronto, Ontario, Canada
Number of Device and Procedure related adverse events
To evaluate the incidence and severity of adverse events (AEs) associated with the ExAblate transcranial treatment
Time frame: At the time of ExAblate transcranial procedure
Severity of Device and Procedure related adverse events
To evaluate the incidence and severity of adverse events (AEs) associated with the ExAblate transcranial treatment
Time frame: At the time of ExAblate transcranial procedure
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