Evaluation intrauterine adhesion after uterine myoma surgery
Not Applicable
- Conditions
- intrauterine synechia.Other specified noninflammatory disorders of uterus
- Registration Number
- IRCT2014123020486N1
- Lead Sponsor
- Research Deputy of Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 40
Inclusion Criteria
all of the married fertile women who had undergone myomectomy; having intra-mural and sub-serosal fibroids; types 3-6 (according to FIGO classification).
Exclusion criteria: receiving GnRH analogous; a history of uterine surgery; the presence of systemic conditions which increase the occurrence rate of synechiae such as genital tuberculosis, endometritis or post-operative fever of unknown origin; no desire to includr in the survey; patients for whom laparoscopy was contra-indicated due to the myoma size or other parameters.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intrauterine synechia. Timepoint: 3 months after myomectomy. Method of measurement: According to the modified classification of the European Society of Gynecological Endoscopy (ESGE).
- Secondary Outcome Measures
Name Time Method Evaluation relationship between type, size and location of myoma with frequency and severity of intrauterine adhesion. Timepoint: 3 months after myomectomy. Method of measurement: Based on FIGO classification.