MedPath

The evaluation of ovarian reserve after uterine artery embolizatio

Not Applicable
Conditions
uerine fibroma and bleeding.
????????? ??????? ???
Registration Number
IRCT201202163461N5
Lead Sponsor
Kermanshah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
66
Inclusion Criteria

age 25-45, sever vaginal bleeding , 16 week mass, anemia and pressure effect caused by uterine fibroma.

exclusion criteria: pelvic malignancy, ovarian patology,pelvic infection,substance media sensitivity.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
FSH level. Timepoint: Third day of month before and third day six month after both procedures. Method of measurement: serum level , mIU/ cc.
Secondary Outcome Measures
NameTimeMethod
umber of dominant follicle between 12-14 days of cycle. Timepoint: Before and 6 month after intervention. Method of measurement: One dominant follicle by sonography.;Hb level. Timepoint: Before and 6 month after intervention. Method of measurement: Blood level.;Duration of hospitalization. Timepoint: hospitalization time. Method of measurement: The number of days hospitalization through intervention.;Time required to return normal activity. Timepoint: The number of weeks to return normal activity. Method of measurement: weeks.;Pain level after intervention. Timepoint: one week after intervention. Method of measurement: 1-10 score.;Cost of procedure. Timepoint: cost of hospitalization and. Method of measurement: Rials.;Repeat intervention. Timepoint: By 6 month after first intervention. Method of measurement: Operation and hormonal drugs.;Patients symptoms. Timepoint: 6 month after intervention. Method of measurement: Hot flash, bleeding,pain,.
© Copyright 2025. All Rights Reserved by MedPath