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Completed

NCT Number: NCT00365989

MR Guided Focused Ultrasound Treatment of Uterine Fibroids With Enhanced Sonication

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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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Toronto General Hospital, Toronto, Ontario, Canada

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About this study

Uterine leiomyoma (fibroids) are the most common neoplasms of the female pelvis. These benign tumors are generally oval in shape, and often highly vascular. On T2 weighted MR imaging exams, or T1 exams with contrast, uterine fibroids are easily identifiable. They occur in 20-25% of women of reproductive age and can cause a variety of problems generally described as either bleeding or mass effects from the fibroid. InSightec has developed an Enhanced Sonication (ES) technique for the ablation of these fibroids. This mode of tissue ablation has been added to the already FDA approved ExAblate system. The goal of this ES technique is to provide an additional treatment tool that will enhance the treatment effect without additional risks while preserving ALL clinical features of the current commercially approved version.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women age 18 or older, who present with symptomatic fibroids
  • Women who have given written informed consent
  • Women who are able and willing to attend all study visits.
  • Patient is pre or peri-menopausal (within 12 months of last menstrual period).
  • Able to communicate sensations during the ExAblate procedure.
  • Uterine fibroids, which are device accessible (i.e., positioned in the uterus such that they can be accessed without being shielded by bowel or bone).
  • Fibroids(s) clearly visible on non-contrast MRI.

Exclusion criteria

  • Women who are pregnant, as confirmed by serum test at time of screening, or urine pregnancy test on the day of treatment
  • Patient who desire to become pregnant in the future.
  • Patients who are breast-feeding.
  • Patients with an active pelvic inflammatory disease (PID)
  • Active local or systemic infection
  • Metallic implants that are incompatible with MRI
  • Known intolerance to the MRI contrast agent (e.g. Gadolinium or Magnevist)
  • Severe claustrophobia that would prevent completion of procedure in the MR unit.
  • Extensive abdominal scarring in the beam pass or dermoid cyst of the ovary anywhere in the treatment path.
  • Known or suspected pelvic carcinoma or pre-malignant conditions, including sarcoma and adenomatous hyperplasia.
  • Pedunculated fibroids.
  • Intrauterine device (IUD) anywhere in the treatment path
  • Undiagnosed vaginal bleeding.

Treatment and study plan

ExAblate Enhanced Sonication

Device

Other names: Magnetic Resonance guided Focused Ultrasound

Primary outcomes

  1. Number of Adverse Events

    Time frame: Within 1 month of treatment

    The study objective is to determine the safety of the new Enhanced Sonication technique and assure no new safety issues are introduced.

Other outcomes

  1. Mean Enhanced Sonication Normalized Thermal Dose Volume

    Time frame: During treatment

    The secondary end point of the study is to evaluate the mean normalized Enhanced Sonication thermal dose volume. Normalized dose volume is a function of the sonication dose volume divided by the energy transmitted measured from the the MR thermometry imaging.

  2. Number of Participants With Adverse Events

    Time frame: Within 1 month of treatment

Sponsors and collaborators

Lead sponsor

InSightec

Industry

Registry information

Official study title

A Clinical Study To Evaluate the Safety and Efficacy of MR Guided Focused Ultrasound Treatment of Uterine Fibroids With Enhanced Sonication Techniques

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
Aug 18, 2006
Registry last updated
Feb 5, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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