Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT01514617

Diffusion -and Perfusion Weighted MRI for Response Prediction of Symptomatic Leiomyomas Following Uterine Artery Embolization

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Universitaire Ziekenhuizen KU Leuven · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

It is known that volumetric response of leiomyomas following uterine artery embolization correlates well with patients clinical outcome. The aim of this study is to assess diffusion -and perfusion weighted MRI for the prediction of volumetric response following uterine artery embolization in patients with symptomatic leiomyomas.

Conditions

Interventions

TypeNameDescription
PROCEDUREDiffusion -and perfusion weighted MRI including iv contrast agent injectionMRI is a technique based on magnetic fields and does not require the use of ionizing radiation. Although there are no known side effects associated with MRI, a few precautions should be taken because of the 3T magnetic field. This implicates that all metal and magnetized objects must be removed from the patients before entering the MRI room. Patients with a pacemaker, a cardiac defibrillator or other implanted conductors/prostheses are for reason not eligible for the study. During the MRI examination, an intravenous contrast agent will be administered. In most cases, patients do not experience any discomfort and the use of this contrast agent is part of the clinical routine.

Timeline

Start date
2012-01-01
Primary completion
2025-12-01
Completion
2025-12-01
First posted
2012-01-23
Last updated
2024-07-10

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT01514617. Inclusion in this directory is not an endorsement.