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

Recruiting now

Conditions studied: Uterine Fibroid

In brief

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 facts

Study ID

NCT05386615

Run by

InSightec

People needed

200

Starts

2016-02-16

Expected to finish

2026-12-31

Last updated by the study team

2025-04-30

Who can join

Age: 18 and older, up to 50. Sex: female. Healthy volunteers: not accepted.

Where it is running

• UCLA — Los Angeles, California, United States (enrolling)
• Stanford University — Stanford, California, United States (enrolling)
• Mayo Clinic — Rochester, Minnesota, United States (enrolling)
• Shanghai No. 1 Hospital — Shanghai, China (enrolling)
• Shanghai No.1 Hospital — Shanghai, China (enrolling)
• Huashan Hospital Affiliated to Fudan University — Shanghai, China

Full record on ClinicalTrials.gov

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