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This is a phase 3 study to determine the safety of the new features to the FDA approved ExAblate device using a new method to ablate fibroids deemed Enhanced Sonication.
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Lead Sponsor
InSightec
NCT05862272 · Uterine Fibroids, Endometriosis
NCT07474688 · Uterine Fibroids (Leiomyoma)
NCT02100904 · Uterine Fibroids
NCT03948789 · Uterine Fibroids
NCT07384468 · Uterine Fibroids (UF)
University of California at San Diego
La Jolla, California
Lahey Clinic
Burlington, Massachusetts
KNI
Kalamazoo, Michigan
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Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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