MedPath

The study of efficacy and complications of uterine artery embolization in patients with symptomatic uterine fibroids

Not Applicable
Conditions
utrine fibroids and bleeding.
Other specified noninflammatory disorders of uterus
Registration Number
IRCT2014012714333N16
Lead Sponsor
Kermanshah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
97
Inclusion Criteria

written consent of the patient; women with symptomatic uterine fibroids; candidate of hysterectomy or myomectomy. Exclusion criteria: no menopause, ovarian tumors.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Type of fibroids. Timepoint: Baseline and 3, 6 and 12 months after embolization (UAE). Method of measurement: MRI.;Uterine size. Timepoint: Baseline and 3, 6 and 12 months after embolization (UAE). Method of measurement: Sonography.;Clinical symptoms. Timepoint: 3, 6 and 12 months after embolization (UAE). Method of measurement: Based on questionnaire.;Fibroid size. Timepoint: Baseline and 3, 6 and 12 months after embolization (UAE). Method of measurement: MRI.;Permanent amenorrhea. Timepoint: Baseline and 3, 6 and 12 months after embolization (UAE). Method of measurement: Asking the patient.;Continuous vaginal discharge. Timepoint: 3, 6 and 12 months after embolization (UAE). Method of measurement: Asking the patient.;Recurrence of fibroids. Timepoint: 3, 6 and 12 months after embolization (UAE). Method of measurement: MRI.
Secondary Outcome Measures
NameTimeMethod
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