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OCL 500 Treatment of Women With Symptomatic Uterine Fibroids

Leiomyoma Clinical Trial

Official title:
An Open Label, Single Center Study to Evaluate the Safety and Effectiveness of OCL 500 Embolization Microspheres (OCL 500) in Uterine Artery Embolization for the Treatment of Premenopausal Women With Symptomatic Uterine Fibroids

Clinical Trial Summary

This is a prospective, open-label, single-arm, safety and effectiveness study of Occlusin 500 microspheres in women with symptomatic uterine fibroids.

Clinical Trial Description

Prior to entering the study, all patients will undergo pre-study assessments including compliance with inclusion and exclusion criteria, laboratory assessments, pelvic examination, and imaging of the pelvis. Following conventional catheter angiography to confirm catheter placement and the uterine vasculature, each patient will undergo transarterial embolization with Occlusin 500 microspheres. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03427671
Study type Interventional
Source IMBiotechnologies Ltd.
Contact
Status Completed
Phase N/A
Start date January 17, 2018
Completion date September 3, 2019
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