MR Guided Focused Ultrasound Surgery in the Treatment of Uterine Fibroids

Uterine Fibroids Clinical Trial

Official title:

Post Approval Study: MR Guided Focused Ultrasound Surgery in the Treatment of Uterine Fibroids

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00166270
• Other study ID #: UF014
• Status: Completed
• Phase: N/A
• Start date: January 2005
• Est. completion date: January 2009

Study information

• Verified date: July 2018
• Source: InSightec
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, nonrandomized, multi-center study to evaluate the safety and effectiveness of ExAblate in the treatment of uterine fibroids. All patients will be treated and then followed for 36 months to evaluate the change in their fibroid symptoms.

Description:

After the PMA Panel, the sponsor was requested to conduct a post-approval study. The objective of this study is to gather additional data to evaluate the safety and long term effectiveness of focused ultrasound treatment, and to include a larger cohort of African-American patients. Patients will be treated following the approved commercial treatment guidelines.

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. In general, these symptoms can be classified into two categories:

1. heavy menstrual bleeding, defined as bleeding on heavy days requiring a change of sanitary wear every 2 hours or less, significant clot passage, flooding, substantial prolongation of menstrual periods compared with the patient's prior experience, or anemia.

2. pelvic pain or pressure, heaviness or discomfort, or similar symptoms in the back, flank or leg attributable to the bulk of the fibroid, urinary frequency, increase in nocturia, difficulty voiding or compression of the ureters with hydronephrosis.

Measures of the clinical success of patients who elect treatment of fibroids are generally subjective, and evaluated by the patient in terms of improvement in the initial symptoms that caused her to seek treatment (decrease in pain, bladder or bowel symptoms, or reduction in vaginal bleeding), while experiencing a minimum of co-morbidities from the treatment itself.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 70
• Est. completion date: January 2009
• Est. primary completion date: April 2006
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Women who present with symptomatic uterine fibroids and are not seeking treatment for the reason of improving fertility.

• Able and willing to give consent and able 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:

• Metallic implants that are incompatible with MRI

• Sensitive to MRI contrast agents

• Severe claustrophobia that would prevent completion of procedure in MR unit

• Who are pregnant or desire to become pregnant in the future. Pregnancies following ExAblate treatment could be dangerous for both mother and fetus.

• Pedunculated fibroids

• Active pelvic inflammatory disease (PID)

• Active local or systemic infection

• Known or suspected pelvic carcinoma or pre-malignant conditions, including sarcoma and adenomatous hyperplasia

• Intrauterine device (IUD) anywhere in the treatment path

• Dermoid cyst of the ovary anywhere in the treatment path

• Extensive abdominal scarring that cannot be avoided by redirection of the beam (e.g., due to Caesarean section or repeated abdominal surgeries)

• Undiagnosed vaginal bleeding

Related Conditions & MeSH terms

• Leiomyoma
• Uterine Fibroids

Intervention

Device:
• ExAblate 2000

Locations

Country	Name	City	State
United States	University MRI	Boca Raton	Florida
United States	Brigham & Women's Hospital	Boston	Massachusetts
United States	Lahey Clinic	Burlington	Massachusetts
United States	Radnet Management	Los Angeles	California
United States	North Texas Uterine Fibroid Institute	Plano	Texas
United States	Virtua	Voorhees	New Jersey

Sponsors (1)

Lead Sponsor	Collaborator
InSightec

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Measures of the clinical success of patients who elect treatment of fibroids are generally subjective, and evaluated by the patient in terms of improvement.		Within 1 month of Treatment

External Links

•   Sponsor web page