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NCT04998864

Assessment of Safety and Feasibility of ExAblate Blood-Brain Barrier (BBB) Disruption in GBM Patients

Sponsor: InSightec

View on ClinicalTrials.gov

Summary

The purpose of this study is to evaluate the safety of the Exablate Model 4000 Type 2.0 used as a tool to disrupt the BBB in patients with high grade glioma undergoing standard of care therapy.

Official title: Assessment of Safety and Feasibility of Exablate Blood-Brain Barrier Disruption for the Treatment of High-Grade Glioma in Patients Undergoing Standard Chemotherapy

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

OBSERVATIONAL

Enrollment

3

Start Date

2021-08-25

Completion Date

2023-10-12

Last Updated

2026-04-16

Healthy Volunteers

No

Interventions

DEVICE

Magnetic Resonance guided Focused ultrasound (MRgFUS)

FUS involves the application of acoustic energy at low frequencies from over 1000 individual transducers into distinct body targets.

Locations (2)

Fondazione IRCCS Neurologico Carlo Besta

Milan, Italy

CINAC-Hospital HM Puerta del Sur

Móstoles, Madrid, Spain