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Clinical Trial Summary

The goal of this study is to validate the new ExAblate Application software V4.2 by developing additional data that shows the safety of this treatment. The ExAblate is intended to ablate uterine fibroid tissue in pre- or peri-menopausal women with symptomatic uterine fibroids who desire a uterine sparing procedure. Patients must have a uterine size of less than 24 weeks and not seeking treatment for reasons of improving fertility.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00295217
Study type Interventional
Source InSightec
Contact
Status Completed
Phase Phase 3
Start date February 2006
Completion date October 2006

See also
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