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Clinical Trial ● Currently Recruiting NCT06153667

Bearing nsPVA Embolization for Uterine Artery Embolization (BETTER-UAE)

Bearing nsPVA Embolization for Uterine Artery Embolization (BETTER-UAE) — Recruiting • Oncology • NCT06153667.

📅 29 May 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
NCT ID
NCT06153667
Sponsor
Merit Medical Systems, Inc.
Start
2024-08-22
ClinicaliQ Trial Snapshot
  • Bearing nsPVA Embolization for Uterine Artery Embolization (BETTER-UAE) — Recruiting • Oncology • NCT06153667.
  • What is being tested: Safety and performance of Bearing nsPVA (non-spherical polyvinyl alcohol) embolization particles as an embolic agent for uterine artery embolization in patients undergoing treatment for uterine fibroids, with follow-up data collected over 6 months.
  • Patient eligibility overview: The study includes subjects who have been selected for and are undergoing uterine fibroid embolization treatment; specific inclusion/exclusion criteria would be defined in the full protocol but generally encompasses patients with symptomatic fibroids suitable for this minimally invasive vascular….
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

This is a prospective, multicenter, observational, post-market clinical follow-up study in subjects treated with Bearing nsPVA Embolization Particles for uterine fibroid embolization. Data collection will include safety and performance outcome relating to the use of Bearing nsPVA, through 6 months.

Eligibility Snapshot
  • : * Adult women ≥ 18 years old at the time of enrollment. * Subject has symptomatic uterine fibroid(s), suitable to embolization. * Subject provides written informed consent.

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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