NCT03900507

Postoperative Results of Incisional Endometriosis

Postoperative Results of Patients Who Received Medical Treatment for Incisional Endometriosis and Did Not Respond to Treatment

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 40 (actual)
• Sponsor: Kanuni Sultan Suleyman Training and Research Hospital · Academic / Other
• Sex: Female
• Age: 18 Years – 45 Years
• Healthy volunteers: —

Summary

The primary aim is to determine the endometriotic foci formed in the incision line after surgical operations, and the medical treatment approach is the primary objective. Medical treatment was initiated and the patients who did not benefit from the treatment would be operated and postoperative pain scores would be compared with the medical treatment. It will be tried to determine which treatment is more effective in pain control. In addition to removing the symptoms and providing therapeutic methods in patients, it is aimed to help in differential diagnosis of dermatological diseases and malignancy and thus to prevent anxiety in patients. It is also aimed to evaluate the pathology results in the most appropriate way to eliminate the symptoms (severe pain, bleeding, etc.) that occur in accordance with the menstrual cycle every month.

Conditions

• Endometriosis
• Pain

Interventions

Type	Name	Description
PROCEDURE	endometriosis surgery	Medical treatment was initiated in patients with abdominal incision due to endometriotic focus in the incision line. however, patients with surgical excision indications were the study group.

Timeline

• Start date: 2018-06-01
• Primary completion: 2019-07-01
• Completion: 2019-07-01
• First posted: 2019-04-03
• Last updated: 2019-07-16

Locations

1 site across 1 country: Turkey (Türkiye)