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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Investigator), Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT01514617
Study type Interventional
Source Universitaire Ziekenhuizen Leuven
Contact
Status Active, not recruiting
Phase N/A
Start date January 2012
Completion date December 2016

See also
  Status Clinical Trial Phase
Completed NCT00839722 - Fertility After Uterine Artery Embolisation for the Treatment of Leiomyomas Phase 2
Withdrawn NCT01553123 - Efficacy and Safety Study of Ulipristal Acetate in Females With Anemia Associated With Uterine Leiomyoma Phase 3
Completed NCT01592903 - Somatic Stem Cells in Leiomyomas? N/A