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OpenTrials
Completed

NCT Number: NCT00354471

Uterine Artery Embolization for Symptomatic Fibroids

This study will evaluate the safety, efficacy , quality of life and patient satisfaction of uterine artery embolization for the treatment of symptomatic uterine fibroids. It will provide useful information in the development od guidelines in patient selection, procedural management and subsequent follow up.

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Key information

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Symptoms related to the pressence of uterine fibroids serious enough to consider surgical options
  • Confirmation of fibroids by endovaginal and transabdominal ultrasound

Exclusion criteria

  • Pedunculated fibroids
  • Desire for fertility
  • Carcinoma of pelvic organs
  • Previous pelvic irradiation
  • Bleeding diathesis and vasculitis
  • History of allergiy to contrst medium

Treatment and study plan

Uterine Artery Embolization

Procedure

Sponsors and collaborators

Lead sponsor

University of Manitoba

Other

Registry information

Official study title

Short and Long Term Outcomes of Uterine Artery Embolization.

Important dates

First posted
Jul 20, 2006
Registry last updated
Feb 5, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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