The effect of ovarian suspension in Endometriosis surgery
Not Applicable
Recruiting
- Conditions
- severe endometriosis.Endometriosis of ovaryN80.1
- Registration Number
- IRCT20120201008897N10
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 70
Inclusion Criteria
Women over 18 years of age who are diagnosed with endometriosis + no sliding according to transvaginal ultrasound and history and physical condition
Women with severe endometriosis need bilateral dissection and need to protect the uterus and ovaries
Patient informed consent to enter the study
Exclusion Criteria
Inability to tolerate transvaginal ultrasound
Unsuccessful surgery
- Patients who suffer from surgical complications such as intestinal injury, unplanned oophorectomy or change to laparotomy
Lack of subsequent patient visits to determine the severity of menstrual pain and postoperative complications
The patient refuses to continue attending the study
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Check for adhesion. Timepoint: Before surgery and three months after surgery. Method of measurement: Transvaginal ultrasound.
- Secondary Outcome Measures
Name Time Method Severity of dysmenorrhea. Timepoint: Before surgery and three months after surgery. Method of measurement: Visual Analogue Scale.;Severe dyspareunia. Timepoint: Before surgery and three months after surgery. Method of measurement: Visual Analogue Scale.;Severe postoperative pain. Timepoint: Up to three days after surgery. Method of measurement: Visual Analogue Scale.;Severity of chronic pelvic pain. Timepoint: Before surgery and three months after surgery. Method of measurement: Visual Analogue Scale.