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The effect of ovarian suspension in Endometriosis surgery

Effectiveness of ovarian suspension in preventing post-operative ovarian adhesion in woman with sever endometriosis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120201008897N10
Enrollment
70
Registered
2022-05-23
Start date
2022-05-22
Completion date
Unknown
Last updated
2022-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

severe endometriosis. Endometriosis of ovary

Interventions

Intervention 1: Intervention group: Women with severe endometriosis, after the release of adhesions during the operation, the ovaries are hung on the anterior wall of the abdomen with vicryl thread an
This period is equivalent to the period of peritoneal repair. Then, three months later, an ultrasound is performed to check for ovarian adhesions. Intervention 2: Control group: Control group: In wome

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Check for adhesion. Timepoint: Before surgery and three months after surgery. Method of measurement: Transvaginal ultrasound.

Secondary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsafoura rouholamin

Esfahan University of Medical Sciences

s_rouholamin@med.mui.ac.ir+98 31 3663 9903

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026