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Recruiting NCT06153667

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

Conditions: Uterine Fibroid

Sponsor: Merit Medical Systems, Inc.

trial.available_in: БГ
Overview
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.
Who can participate
Inclusion Criteria: * Adult women ≥ 18 years old at the time of enrollment. * Subject has symptomatic uterine fibroid(s), suitable to embolization. * Subject provides written informed consent. Exclusion Criteria: * Subject is pregnant. * Subject has suspected pelvic inflammatory disease or any other pelvic infection. * Subject has any malignancy of the pelvic region, (e.g., endometrial neoplasia).
Locations 3
Australia (1)
The Wesley Hospital
Brisbane
United Kingdom (1)
Royal Gwent Hospital (Aneurin Bevan UHB)
Newport
United States (1)
Astra Vascular/Astra Vein Treatment Center
Brooklyn , New York
Technical details
Status
Recruiting
Study type
OBSERVATIONAL
Sex
Female only
Minimum age
18 Years
Healthy volunteers
No
Start date
22.08.2024
Completion date
01.12.2026
Registry ID
NCT06153667
Source
anzctr
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