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Clinical trialNCT00365989CompletedPhase 3Interventional

MR Guided Focused Ultrasound Treatment of Uterine Fibroids With Enhanced Sonication

SponsorInSightecEnrollment50Uterine FibroidsUterine Leiomyoma
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

5 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Canada
  • Toronto General Hospital

    Toronto, Ontario, Canada

United States
  • University of California at San Diego

    La Jolla, California, United States

  • Lahey Clinic

    Burlington, Massachusetts, United States

  • Kni

    Kalamazoo, Michigan, United States

  • Cornell Vascular

    New York, New York, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Oct 2006
Primary completion
31 Aug 2008
Completion
31 Aug 2008
Last update posted
5 Feb 2019
Registered enrollment
50
Registry id
NCT00365989

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 11 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.