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Spots Global Cancer Trial Database for Blood-Brain Barrier Disruption (BBBD) for Liquid Biopsy in Subjects With GlioBlastoma Brain Tumors

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Trial Identification

Brief Title: Blood-Brain Barrier Disruption (BBBD) for Liquid Biopsy in Subjects With GlioBlastoma Brain Tumors

Official Title: A Pivotal Study to Evaluate the Safety and Effectiveness of Exablate Model 4000 Using Microbubble Resonators to Temporarily Mediate Blood-Brain Barrier Disruption (BBBD) for Liquid Biopsy in Subjects With GlioBlastoma Brain Tumors

Study ID: NCT05383872

Study Description

Brief Summary: The purpose of this study is to evaluate the safety and efficacy of targeted blood brain barrier disruption with Exablate Model 4000 Type 2.0/2.1 for liquid biopsy in subjects with suspected Glioblastoma brain tumors

Detailed Description: This is a prospective, multi-center, pivotal clinical trial to evaluate the safety and efficacy of targeted blood brain barrier disruption using Exablate Model 4000 Type 2 for liquid biopsy in subjects with suspected Glioblastoma brain tumors. The study will be conducted at up to 25 centers in the US.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of California, Los Angeles, Los Angeles, California, United States

University of California San Francisco, San Francisco, California, United States

UF Health Shands Hospital, Gainesville, Florida, United States

Miami Cancer Institute at Baptist Health, Miami, Florida, United States

Tampa General Hospital, Tampa, Florida, United States

University of Maryland, Baltimore & The University of Maryland Medical System, Baltimore, Maryland, United States

Johns Hopkins University, Baltimore, Maryland, United States

Mayo Clinic, Rochester, Minnesota, United States

NYU Grossman School of Medicine, New York, New York, United States

Duke University, Durham, North Carolina, United States

University of Pennsylvania, Philadelphia, Pennsylvania, United States

University of Texas, Southwestern, Dallas, Texas, United States

University of Texas MD Anderson Cancer Center, Houston, Texas, United States

West Virginia University Rockefeller Neuroscience Center, Morgantown, West Virginia, United States

Sunnybrook Research Institute, Toronto, Ontario, Canada

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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