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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


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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