Safety Study of ExAblate for the Treatment of Uterine Fibroids

Not Applicable

Completed

Brief Summary: The objective of this Phase IV study is to evaluate the safety of the ExAblate treatment of uterine fibroids using the enhanced sonication techniques, based on the current commercially-approved treatment guidelines. Treatment may include up to 100% of individual fibroid volume, within established serosal and sacral treatment margins.

The Enhanced sonication is one of the various sonication modes that may lead to increased thermal dose volume of each sonication without additional safety risks. This is an additional treatment tool available in the ExAblate system for the treatment of uterine fibroids.

The safety profile of the Enhanced Sonication was investigated under an FDA-regulated IDE study. FDA granted approval of Enhanced Sonication with the requirement to perform a post-approval study to collect additional safety data when treating up to 100% of individual fibroid volume.

Recruitment & Eligibility

Inclusion Criteria

Women age 18 or older
Symptomatic uterine fibroids, defined as those resulting in scores of 21 or higher, based on patient responses to questions 1-8 of the Uterine Fibroid Symptom and Health-Related Quality of Life Questionnaire (UFS-QOL)
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).
Patient should be family complete.
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.
Fibroid enhances on MR contrast imaging.

Exclusion Criteria

Women who are pregnant, as confirmed by serum/urine test at time of screening, or urine pregnancy test on the day of treatment.
Patients who are breast-feeding.
Patients with active pelvic inflammatory disease (PID).
Patients with active local or systemic infection.
Patients experiencing chronic leg or lower back pain within the last 6 months.
Contraindication for MRI Scan:
- Severe claustrophobia that would prevent completion of procedure in the MR unit
- Weight greater than 250 lbs (113Kg)
- Implanted ferromagnetic materials and/or devices contraindicated for MR scan
- Known intolerance to MRI contrast agent (e.g. Gadolinium or Magnevist)
- Any other contraindication for MRI Scan
Extensive abdominal scarring in the beam path (that cannot be avoided by redirection of the beam).
Dermoid cyst of the ovary anywhere in the treatment path.
Known or suspected pelvic carcinoma or pre-malignant conditions, including sarcoma and adenomatous hyperplasia.
Intrauterine device (IUD) anywhere in the treatment path.
Undiagnosed vaginal bleeding.
Pedunculated fibroids.
Uterine size >24 weeks.

Arm && Interventions

Group	Intervention	Description
ExAblate treatment	ExAblate	-

Primary Outcome Measures

Name	Time	Method
Percent Occurrence of Chronic Leg Pain	From treatment to 1-month post-treatment	The hypothesis was that over 90% of subjects would not experience chronic leg pain. A lower 95% Confidence Limit \> 0.90 was considered statistically successful.

Secondary Outcome Measures

Name	Time	Method

Locations (8): Borgess Research Institute
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Kalamazoo, Michigan, United States
Duke University
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Durham, North Carolina, United States
University Image Guided Therapy
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Boca Raton, Florida, United States
University of Virginia Health System
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Charlottesville, Virginia, United States
UCLA
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Los Angeles, California, United States
UCSD Department of Radiology
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San Diego, California, United States
University of California San Francisco
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San Francisco, California, United States
The Methodist Hospital Research Institute
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Houston, Texas, United States