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RECRUITING
NCT05386615
Post-Exablate Pregnancy Outcomes Registry Study: Exablate Treatment of Symptomatic Uterine Fibroids
Sponsor: InSightec
View on ClinicalTrials.gov
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.
Key Details
Gender
FEMALE
Age Range
18 Years - 50 Years
Study Type
OBSERVATIONAL
Enrollment
200
Start Date
2016-02-16
Completion Date
2026-12-31
Last Updated
2025-04-30
Healthy Volunteers
No
Conditions
Interventions
DEVICE
Body System - Functional
MR-Guided Focused Ultrasound
Locations (6)
UCLA
Los Angeles, California, United States
Stanford University
Stanford, California, United States
Mayo Clinic
Rochester, Minnesota, United States
Huashan Hospital Affiliated to Fudan University
Shanghai, China
Shanghai No. 1 Hospital
Shanghai, China
Shanghai No.1 Hospital
Shanghai, China