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Clinical trialNCT01504308TerminatedPhase 2/PHASE3Interventional

Sonalleve Fibroid Ablation Pivotal Clinical Trial for MR-HIFU of Uterine Fibroids

SponsorPhilips HealthcareEnrollment49Uterine Fibroids
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this clinical study is to determine whether treatment with the Philips Sonalleve Magnetic Resonance-guided High Intensity Focused Ultrasound (MR-HIFU) system is effective in the treatment symptomatic uterine leiomyomas (uterine fibroids).

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

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

Canada
  • Sunnybrook Health Sciences Centre

    Toronto, Ontario, Canada

South Korea
  • Samsung Medical Center

    Seoul, South Korea

United States
  • University of Chicago

    Chicago, Illinois, United States

  • University of Michigan

    Ann Arbor, Michigan, United States

  • Montefiore Medical Center

    The Bronx, New York, United States

  • Oregon Science and Health University

    Portland, Oregon, United States

  • Vanderbilt Medical Center

    Nashville, Tennessee, United States

  • University of Texas Southwestern Medical Center

    Dallas, Texas, United States

  • St. Luke'S Episcopal Hospital

    Houston, Texas, 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 May 2012
Primary completion
31 Mar 2016
Completion
31 Mar 2016
Last update posted
5 Apr 2017
Registered enrollment
49
Registry id
NCT01504308

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.