🏛️ Verified NIH Record • Updated 2025-04-29
Post-Exablate Pregnancy Outcomes Registry Study: Exablate Treatment of Symptomatic Uterine Fibroids (NCT05386615)
🟢 Recruiting Interventional Protocol 📊 Observational Clinical Research Sponsor: InSightec
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: UCLA — Los Angeles, California
Age range: 18 Years to 50 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (6 Sites)
- UCLA — Los Angeles, California
- Stanford University — Stanford, California
- Mayo Clinic — Rochester, Minnesota
- Huashan Hospital Affiliated to Fudan University — Shanghai,
- Shanghai No. 1 Hospital — Shanghai,
- Shanghai No.1 Hospital — Shanghai,
📞 Contact the Study Coordinator
Phone: (214) 630-2000
Email: nadira@insightec.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Uterine Fibroid
- Life Study: Lifestyle Intervention in Fibroid Elimination — New York, New York
- Ascertaining Longterm Outcomes of Fibroid Treatments — San Francisco, California
- Evaluation of Uterine Fibroids by CEUS and SHAPE Pre and Post UAE — Philadelphia, Pennsylvania
- Bearing nsPVA Embolization for Uterine Artery Embolization (BETTER-UAE) — Brooklyn, New York
Explore by condition: All Uterine Fibroid clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.