Clinical Trials in the USA / NCT05386615
Recruiting
Observational
Post-Exablate Pregnancy Outcomes Registry Study: Exablate Treatment of Symptomatic Uterine Fibroids
NCT05386615 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Uterine Fibroid
Investigational drug(s) / intervention(s)
Body System - Functional
Body System - Functional: MR-Guided Focused Ultrasound
Study 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.
Eligibility
Inclusion Criteria: - - Eligibility is as per the symptomatic fibroids device indication. - All registry-consented patients following the treatment of their fibroid(s) with the Exablate system. Exclusion Criteria: -
Primary outcome measure(s)
- Occurrence of adverse events — Through study completion, an average of 2 years.
All adverse events and/or serious adverse events will be documented and reported according to protocol.
Trial sites (6)
| Facility | City | Region | Status |
|---|---|---|---|
| UCLA | Los Angeles | California | Recruiting |
| Stanford University | Stanford | California | Recruiting |
| Mayo Clinic | Rochester | Minnesota | Recruiting |
| Huashan Hospital Affiliated to Fudan University | Shanghai | China | Active Not Recruiting |
| Shanghai No. 1 Hospital | Shanghai | China | Recruiting |
| Shanghai No.1 Hospital | Shanghai | China | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05386615 on ClinicalTrials.gov ↗ ← All trials in the USA