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Clinical Trials/NCT04062916
NCT04062916
Completed
Not Applicable

Improvement in Quality of Life and Pain Scores After Laparoscopic Management of Deep Infiltrating Endometriosis

Acibadem Fulya Hastanesi1 site in 1 country65 target enrollmentJanuary 2013
ConditionsEndometriosis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endometriosis
Sponsor
Acibadem Fulya Hastanesi
Enrollment
65
Locations
1
Primary Endpoint
Pain levels after endometriosis surgery
Status
Completed
Last Updated
6 years ago

Overview

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 endometrioma and DIE together; who underwent a laparoscopic surgery by a team of gynecologists, colorectal surgeons, and a urologist were retrospectively evaluated. The data were collected in a specific database and analyzed for postoperative pain outcomes through a comparison with preoperative symptoms scored using a visual analogue score (VAS), and the British Society of Gynecologic Endoscopy (BSGE) pelvic pain questionnaire.

Registry
clinicaltrials.gov
Start Date
January 2013
End Date
June 2019
Last Updated
6 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Acibadem Fulya Hastanesi
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 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 Criteria

  • \*Any other endometriosis patient that do no meet the inclusion criteria

Outcomes

Primary Outcomes

Pain levels after endometriosis surgery

Time Frame: 3 years

Effects of endometriosis surgery on pelvic pain by using VAS scores

Quality of Life after endometriosis surgery

Time Frame: 7 years

Effects of endometriosis surgery on the quality of life by using BSGE pelvic pain questionnaire

Study Sites (1)

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