Uterine Fibroids Clinical Trial
Official title:
Short and Long Term Outcomes of Uterine Artery Embolization.
NCT number | NCT00354471 |
Other study ID # | B2000 115 |
Secondary ID | |
Status | Completed |
Phase | Phase 3 |
First received | July 19, 2006 |
Last updated | February 4, 2009 |
Verified date | July 2006 |
Source | University of Manitoba |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Health Canada |
Study type | Observational |
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.
Status | Completed |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Female |
Age group | 18 Years to 60 Years |
Eligibility |
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 |
Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Canada | Health Sciences Centre | Winnipeg | Manitoba |
Lead Sponsor | Collaborator |
---|---|
University of Manitoba |
Canada,
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