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Post-Exablate Pregnancy Outcomes Registry Study: Exablate Treatment of Symptomatic Uterine Fibroids

Uterine Fibroid Clinical Trial

Official title:
Post-Exablate Pregnancy Outcomes Registry Study: Exablate Treatment of Symptomatic Uterine Fibroids

Clinical Trial Summary

The goal of this Registry Study is to capture clinical pregnancy outcomes and fibroid treatment background data for any subject post-Exablate treatment for their symptomatic fibroids.

Clinical Trial Description

This is an observational study only for all consented subjects who undergo an Exablate treatment. The Exablate procedure is a commercial treatment. The objective of this registry is to collect data about the effect of Exablate treatment on potential pregnancy occurrences in this population for two years post-treatment for purposes of labeling updates and overall safety data collection. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05386615
Study type Observational [Patient Registry]
Source InSightec
Contact Nadir Alikacem
Phone +12146302000
Email nadira@insightec.com
Status Recruiting
Phase
Start date February 16, 2016
Completion date December 31, 2023
View Details
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