Bowel ENDOmetriosis; Evaluation of Diagnostics and Quality of Life

Sponsor
Oslo University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03779256
Collaborator
St John of God Hospital, Vienna (Other), Nepean Blue Mountains Local Health District (Other)
207
3
26.9
69
2.6

Study Details

Study Description

Brief Summary

Endometriosis on the bowel is a benign condition that can cause major complaints and severely affect the quality of life of women of fertile age. If medical treatment is not enough to improve pain and/or other symptoms it may be necessary to undergo major surgical treatment and removal of the endometriosis nodule on the bowel. Such extensive surgical treatment carries risks of serious complications. Therefore, a thorough diagnostic work-up before surgery is important to know the extent of disease. This will provide women with the best possible information and for the surgeon to plan the operation. The risk of complications increases as the bowel endometriosis is localized closer to the anus as well and/or if the bowel nodule is large.

The distance between the anus and the nodule and the size of the nodule can be measured with two dimensional (2D) vaginal ultrasound. Additionally, Magnetic resonance imaging (MRI) is also used in some countries for these same measurements. Our study would like to investigate the diagnostic value of 2D ultrasound and MRI as well as learn more about women's quality of life before and after surgery. The investigators have designed the study to evaluate the following three questions into three studies ENDO1, ENDO2 and ENDO3:

  • ENDO1: How good is 2D transvaginal ultrasound at measuring the size of the bowel endometriosis nodule and the distance between anus and the lower part of the bowel nodule compared to measurements done during surgery?

  • ENDO2: What is the quality of life, sexual and bowel function of women before and 3- and 12-months after surgery due to bowel endometriosis? Questionnaires will be used.

  • ENDO3: How good is 2D transvaginal ultrasound at measuring the size of the bowel endometriosis nodule compared to magnetic resonance imaging (MRI) and measurements done during surgery?

Condition or Disease Intervention/Treatment Phase
  • Procedure: 2D transvaginal ultrasound

Detailed Description

Mild endometriosis normally affects the peritoneum. More advanced form of endometriosis is termed deep infiltrating endometriosis (DIE). In women suffering from DIE, the endometriotic tissue invades the tissue >5mm below the peritoneal surface, affecting organs in the pelvis like the ovaries, uterus, vagina, bladder, ureters and/or bowel. In women with suspected endometriosis, the prevalence of DIE affecting the bowel is found to range from 24.0 to 73.3%. The symptoms of DIE can be debilitating with dysmenorrhoea, dyspareunia, altered bowel motions, dyschezia and/or dysuria. Thus, it may have an immense impact on women's quality of life with societal consequences.

The risk of complications with surgery for deep infiltrating endometriosis (DIE) of the bowel can be severe like anastomotic leak and rectovaginal fistula. Evidence show that there is an increased risk of anastomotic leaks bowel if the anastomosis <5-8cm from the anal verge. DIE of the rectosigmoid colon can be diagnosed by widely available and low-cost two-dimensional transvaginal sonograhpy (2D-TVS) with a high sensitivity and specificity. MRI is comparable to TVS in diagnosis of intestinal endometriosis but is costlier and less available than TVS. MRI has the advantage over 2D-TVS that it is reproducible, the area of interest can be viewed in many planes and the images can be reviewed and compared by same or different examiners over time.

There are two surgical approaches used in women suffering from bowel endometriosis, namely segmental resection of rectosigmoid or nodule excision. Nodule excision may be performed by shaving (not opening the rectum) or disc excision (removing bowel nodule with surrounding rectal wall). The success of pelvic pain reduction following surgery in women suffering from DIE is related to the radicality of surgery. However, some argue a more symptom-guided approach to surgery.

Endometriosis itself and surgical treatment may have immense impact endometriosis can have on a woman's life. Thus, it is essential to discuss the severity of symptoms, any implications of surgery as well as the risk of complications to enable women informed consent. The pre-operative information and decision making is based on symptoms, fertility wish, the clinical examination and diagnostic tests. Consequently, diagnostic tools such as TVS and MRI are important factors to plan and perform a safe procedure with the best possible outcomes for the women.

There are, to the investigator's knowledge, no studies, which demonstrate if there is a correlation between measurement of the size of an endometriotic rectosigmoid lesion with 2D-TVS compared to the actual lesion size in the resected bowel. Additionally, there are no studies that investigate the correlation between the distance between the rectosigmoid lesion and the anal verge, to plan appropriate surgery and estimate risk of serious complications. Furthermore, there are no known studies evaluating the correlation of measurements of bowel lesions when comparing transvaginal 2D-TVS, MRI and surgery. The aim of surgery is to improve women's quality of life and thus it is essential to evaluate results before and after surgery for bowel endometriosis.

Study Design

Study Type:
Observational
Actual Enrollment :
207 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
ENDO - Bowel ENDOmetriosis; Evaluation of Diagnostics and Quality of Life (ENDO1, ENDO2, ENDO3)
Actual Study Start Date :
Dec 10, 2018
Actual Primary Completion Date :
Jan 10, 2020
Actual Study Completion Date :
Mar 8, 2021

Arms and Interventions

Arm Intervention/Treatment
Women with bowel endometriosis.

Women with symptomatic bowel endometriosis scheduled for surgical treatment investigated with 2D transvaginal ultrasound before surgery at Hospital St John of God, Vienna, Austria; Oslo university hospital, Oslo, Norway and Nepean Hospital, Sydney, Australia. The women recruited at Oslo university hospital, Norway will also have a magnetic resonance imaging (MRI) of the abdomen and pelvis before surger.

Procedure: 2D transvaginal ultrasound
Transvaginal ultrasound is part of routine pre-operative examination of the women before surgery is scheduled. Described surgical treatment interventions is standard practice used to alleviate patient symptoms. Women recruited at Oslo university hospital, Norway will also have an MRI performed pre-operatively.
Other Names:
  • Segmental bowel resection or
  • Disc excision of bowel
  • Outcome Measures

    Primary Outcome Measures

    1. ENDO1AMeasurements on the distance between the lower margin of the rectal lesion and anal verge with 2D-TVS [Before scheduled surgery]

      Millimeter distance measured on 2D TVS

    2. ENDO1A: Measurements on the distance between the lower margin of the rectal lesion and anal verge [During scheduled surgery]

      Millimeter distance measured during surgery

    3. ENDO1B: Size of bowel lesion measured on the excised bowel lesion. [During surgery.]

      Millimeter measurements of the bowel lesion in three orthogonal planes i.e. mid-sagittal, anteroposterior and transverse according to the IDEA group.

    4. ENDO1B: Size of bowel lesion measured with 2D-TVS. [Before scheduled surgery.]

      Millimeter measurements of the bowel lesion in three orthogonal planes i.e. mid-sagittal, anteroposterior and transverse according to the IDEA group.

    5. ENDO2: Incidence of low anterior resection syndrome (LARS) [Preoperatively, 3- and 12-months postoperatively]

      LARS questionnaire consisting of five questions, each response correlates to a score. Lowest score is 0-20 i.e. no LARS, score 21-29 i.e. minor LARS and score 30-42 i.e. major LARS.

    6. ENDO3: Correlation between Lesion to anal verge distance (LAVD) measured with 2D-TVS, MRI and measurements during surgery [Pre-operatively and during surgery]

      Millimeters of lesion to anal verge distance measured

    7. ENDO3: Measurements of bowel lesion size with MRI compared to 2D TVS and surgery [Before and during scheduled surgery]

      Millimeter measurements of the bowel lesion in three orthogonal planes i.e. mid-sagittal, anteroposterior and transverse according to the IDEA group.

    Secondary Outcome Measures

    1. ENDO1: Numerical analogue scale (NAS) score of dysmenorrhea, dyspareunia, dyschezia, dysuria. [Preoperatively, 3 and 12 months postoperatively]

      Numerical analogue scale ranging from 0 to 10 scored for each symptom, 0 representing no pain and 10 representing worst possible pain

    2. ENDO1: Type and frequency of complications after bowel surgery [Through study completion, an average of 1 year]

      "Clavien-Dindo" classification of surgical complications

    3. ENDO2: Quality of life Endometriosis Health Profile-30 [Preoperatively, 3 and 12 months postoperatively]

      Using questionnaire - Endometriosis Health Profile (EHP-30), consisting of a core questionnaire with 30 items grouped into 5 scales and modular questionnaire consisting of 23 items grouped into 6 scales. All scales have a minimum score of 0 (indicating low disability) and a maximum score of 100 (indicating high disability).

    4. ENDO2: Sexual function [Preoperatively, 3 and 12 months postoperatively]

      Using questionnaire - Female Sexual Function Index (FSFI) consisting of 19 questions, minimum score 2.0 (worst score), maximum score 36.0 (best score).

    5. ENDO2: Quality of life before bowel surgery [Before surgery]

      GIQLI (gastrointestinal quality of life index) questionnaire. 36 questions, each containing 4 answers equating to a score ranging from 0 (least desirable answer) to 4 (most desirable answer). Total score range 0-144.

    6. ENDO2: Quality of life after bowel surgery [3 months]

      GIQLI questionnaire

    7. ENDO2: Quality of life after bowel surgery [12 months]

      GIQLI questionnaire

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 50 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Women of reproductive age, ≥ 18 years old, scheduled for planned laparoscopic or open bowel surgery for deep infiltrating endometriosis with suspected symptomatic bowel lesions.
    Exclusion Criteria:
    • Postmenopausal women, women < 18 years old, women with previous bowel surgery. Women who do not speak and read fluent English or Norwegian.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Nepean Hospital Sydney Australia NSW2747
    2 Hospital St John of God Vienna Austria 1020
    3 Oslo university hospital Oslo Norway 0424

    Sponsors and Collaborators

    • Oslo University Hospital
    • St John of God Hospital, Vienna
    • Nepean Blue Mountains Local Health District

    Investigators

    • Principal Investigator: Mee Kristine Aas-Eng, MD, Oslo University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Kristine Aas-Eng, Principal investigator, Oslo University Hospital
    ClinicalTrials.gov Identifier:
    NCT03779256
    Other Study ID Numbers:
    • 2017/1925 REK Sør-Øst D
    First Posted:
    Dec 19, 2018
    Last Update Posted:
    Mar 10, 2021
    Last Verified:
    Mar 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Kristine Aas-Eng, Principal investigator, Oslo University Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 10, 2021