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Study identifier: NCT05386615 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Uterine Fibroid  ·  Sponsor: InSightec

PhaseN/A
Planned participants200
Who can joinFemale, 18 Years to 50 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Nadir Alikacem  ·  +12146302000  ·  nadira@insightec.com

Always discuss trial participation with your own doctor first.

Locations (6)

UCLALos Angeles, California, United StatesRecruiting
Stanford UniversityStanford, California, United StatesRecruiting
Mayo ClinicRochester, Minnesota, United StatesRecruiting
Huashan Hospital Affiliated to Fudan UniversityShanghai, ChinaActive Not Recruiting
Shanghai No. 1 HospitalShanghai, ChinaRecruiting
Shanghai No.1 HospitalShanghai, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05386615