Status:
COMPLETED
Improvement in Quality of Life and Pain Scores After Laparoscopic Management of Deep Infiltrating Endometriosis
Lead Sponsor:
Acibadem Fulya Hastanesi
Conditions:
Endometriosis
Eligibility:
FEMALE
22-50 years
Brief Summary
This is a retrospective cohort study that evaluates the postoperative pain findings of a consecutive series of laparoscopic surgeries for deep infiltrating endometriosis (DIE).
Detailed Description
The study was carried out in university hospitals (Istanbul, Turkey). Patients diagnosed through bimanual gynecologic examination, gynecologic ultrasound or magnetic resonance imaging-confirmed endome...
Eligibility Criteria
Inclusion
- Patients with deep infiltration endometriosis and endometrioma diagnosed through bimanual gynecologic examination, gynecologic ultrasound or through laparoscopically confirmed endometrioma and DIE together;
- DIE with bowel involvement that required shaving or segmental resection for colorectal lesions and nodules;
- Who completed the VAS score and BSGE questionnaire;
- Follow-up period of at least 3 months;
- Patients resistant to medical therapy (NSAIDs, OCPs, levonorgestrel-releasing intrauterine device (IUD), and progesterone) or refuse to use medical therapy.
Exclusion
- \*Any other endometriosis patient that do no meet the inclusion criteria
Key Trial Info
Start Date :
January 1 2013
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
June 1 2019
Estimated Enrollment :
65 Patients enrolled
Trial Details
Trial ID
NCT04062916
Start Date
January 1 2013
End Date
June 1 2019
Last Update
August 20 2019
Active Locations (1)
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1
Acibadem Fulya Hospital
Istanbul, Turkey (Türkiye)