The Impact of NOSE-colectomy on Fertility and Quality of Life Among Patients With Colorectal Endometriosis (NOSERES)
Primary Purpose
Endometriosis, Quality of Life
Status
Completed
Phase
Not Applicable
Locations
Hungary
Study Type
Interventional
Intervention
Surgical procedures( conventional laparoscopic and NOSE technique) for the treatment of colorectal DIE
Sponsored by
About this trial
This is an interventional treatment trial for Endometriosis focused on measuring Fertility, Colorectal endometriosis, Surgery
Eligibility Criteria
Inclusion criteria:
- Age: 18 - 45 years (both inclusive)
- Complaining of infertility and/or pain
Deep endometriosis infiltrating the rectum on at least one imaging technique or confirmed by previous surgery
- up to 15 cm from the anus
- Involving at least the muscularis layer in depth
Exclusion criteria
A potential subject who meets any of the following criteria will be excluded from participation in this study:
- Suspected pelvic malignancy
- Pregnancy
- Patients without bowel resection
Sites / Locations
- Semmelweis University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Patients operated with conventional laparoscopic technique
Patients operated with NOSE laparoscopic technique
Arm Description
Patients operated with conventional laparoscopic technique for colorectal DIE
Patients operated with NOSE technique for colorectal DIE
Outcomes
Primary Outcome Measures
Endometriosis Health Profile, EHP 30
To describe the difference in patient reported outcomes after conventional segmental bowel resection treatment in comparison to NOSE colectomy in patients with deep endometriosis infiltrating the rectum.
The patients are asked to fill the questionnaires preoperatively, at 30 days, 6 months, 1 year and 2 years after the surgery. During the present study investigators are planning an average follow-up of 24 months.
Impact of surgical technique on the quality of life. The outcome will be assessed using validated electronic questionnaires containing questions from Endometriosis Health Profile 30. This is a core questionnaire which consists of five scales (pain, control and powerlessness, emotional well-being, social support, and self-image) contains a total of 30 items. (10)
Gastrointestinal Quality of Life Index, GIQLI
To describe the difference in patient reported outcomes after conventional segmental bowel resection treatment in comparison to NOSE colectomy in patients with deep endometriosis infiltrating the rectum.
The patients are asked to fill the questionnaires preoperatively, at 30 days, 6 months, 1 year and 2 years after the surgery. During the present study investigators are planning an average follow-up of 24 months.
GIQLI is a 36-item patient reported outcomes instrument designed to assess GI-specific health-related quality of life in clinical practice of patients with gastrointestinal disorders. It has five domains (GI symptoms, emotion, physical function, social function and medical treatment) and subscores range from 0-4 while the total score range from 0-144. Higher scores mean better GI health-related quality of life. (11)
LARS score before and after colorectal resection for DIE
To describe the difference in patient reported outcomes after conventional segmental bowel resection treatment in comparison to NOSE colectomy in patients with deep endometriosis infiltrating the rectum.
The patients are asked to fill the questionnaires preoperatively, at 30 days, 6 months, 1 year and 2 years after the surgery. During the present study investigators are planning an average follow-up of 24 months.
The Low Anterior Resection Syndrome (LARS) is a common complication that occures after colorectal surgery. The LARS score is a simple self-administered questionnaire measuring bowel dysfunction after rectal surgery. Contains questions regarding incontinence, emptying difficulties, urgency, and frequency. The calculated score ranges from 0 to 42, with a score of 0-20 representing no LARS, a score of 21-29 representing minor LARS and a score of 30-42 representing major LARS. (12)
Endometriosis related pain before and after colorectal resection for DIE
To describe the difference in patient reported outcomes after conventional segmental bowel resection treatment in comparison to NOSE colectomy in patients with deep endometriosis infiltrating the rectum.
The patients are asked to fill the questionnaires preoperatively, at 30 days, 6 months, 1 year and 2 years after the surgery. During the present study investigators are planning an average follow-up of 24 months.
For the assessment of pre- and postoperative pain a Visual Analogue Scale is used (from 1-10, where 1 is the lowest and 10 is the maximum score) to assess the pre- and postoperative quality of life (dysmenorrhoea, dyspareunia, dyschezia, dysuria, CPP) (13).
Infertility outcomes after colorectal resection for bowel endometriosis
Number of pregnancies, cumulative pregnancy rate and take home baby rate after laparoscopic bowel resection.
Psychological questionnaires:
To describe the difference in patient reported outcomes after conventional segmental bowel resection treatment in comparison to NOSE colectomy in patients with deep endometriosis infiltrating the rectum.
The patients are asked to fill the questionnaires preoperatively, at 30 days, 6 months, 1 year and 2 years after the surgery. During the present study investigators are planning an average follow-up of 24 months.
Pain catastrophizing Scale, Self-Efficacy for Managing Chronic Disease 6-item Scale to investigate the psychological aspect of the disease (14,15).
Secondary Outcome Measures
Complication rates after conventional and NOSE-colectomy performed for colorectal endometriosis
To measure the complication rates after conventional and NOSE-colectomy performed for colorectal endometriosis. The complication rates between the NOSE vs conventional specimen extraction technique will be examined. The difference between the complication rates will be presented according to Clavien-Dindo Classification System (16).
As follows:
Grade I Any deviation from the normal postoperative course without treatment by invasive interventions Grade II Requiring pharmacological treatment with drugs other than such allowed for grade I complications.
Grade III
Requiring surgical, endoscopic or radiological intervention
IIIa
Intervention not under general anesthesia
IIIb
Intervention under general anesthesia Grade IV
Life-threatening complication requiring IC/ICU-management
IVa
single organ dysfunction (including dialysis)
IVb
multiorgan dysfunction Grade V Death of a patient
Hospital stay after colorectal resection perfomed for the treatment of bowel endometriosis
To measure the hospital stay after colorectal resection perfomed for the treatment of bowel endometriosis
Lenght of recovery after colorectal resection performed for the treatment of bowel endometriosis
To measure the lenght of recovery after bowel resection will be assessed by the comparison of the hospital stay (mean +/- SD days)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04109378
Brief Title
The Impact of NOSE-colectomy on Fertility and Quality of Life Among Patients With Colorectal Endometriosis
Acronym
NOSERES
Official Title
The Impact of NOSE-colectomy on Fertility and Quality of Life Among Patients With Colorectal Endometriosis
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
September 1, 2019 (Actual)
Primary Completion Date
March 23, 2021 (Actual)
Study Completion Date
March 23, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Semmelweis University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Deep infiltrating endometriosis (DIE) represents the most severe form of endometriosis and is present in 20-35% of all women suffering from the disease. Intestinal nodules are observed in 3% to 37% of endometriosis patients. In cases of colorectal DIE, adequate therapy depends on the depth of infiltration and the size of the lesion as well as the woman's quality of life. Removal of the specimen after segmental bowel resection can be performed by either mini-laparotomy or by the natural orifice specimen extraction (NOSE) technique .
The assessment of the quality of life and fertility outcome of the patients was done by using electronic questionnaires before and after surgery.
Detailed Description
Endometriosis is an enigmatic disease affecting 6-10% of women of reproductive age or 176 millions of women worldwide (1). Endometriosis is defined as the presence of endometrial-like tissue outside the uterus and it induces a chronic inflammatory reaction (2). Deep infiltrating endometriosis (DIE) represents the most severe form of endometriosis (described by the invasion of anatomical structures and organs deeper than 5 mm beyond the peritoneum) and is present in 20-35% of all women suffering from the disease (3). Intestinal deep infiltrating endometriosis is known as lesions infiltrating at least the muscular layer of the bowel wall and most commonly affects the rectum, sigmoid colon and the rectovaginal septum. (4).
Even if bowel endometriosis may be totally asymptomatic, in many patients intestinal wall DIE alters significantly quality of life by provoking constipation, diarrhea, hematochezia, intestinal cramping, abdominal bloating, intestinal stenosis or obstruction and pain of defecation (5, 6). Rectal fixation to adjacent structures results in angulation of the rectum and subsequent defecatory pain and constipation. Fibrosis of nodules can lead to rectal constriction and stenosis, cyclical inflammation of the rectal wall may lead to changes in bowel habit (usually diarrhoea) with or without rectal bleeding (7).
Although the surgical laparoscopic management of endometriosis is widely accepted, the optimal type of resection, whether conservative approach (shaving, disc resection) or radical technique (involves limited resection of the bowel wall with preservation of all adjacent structures-autonomic pelvic plexus, rectal vascular supply- known as "nerve-vessel sparing limited segmental resection"), is under discussion for treatment of deep endometriosis infiltrating the rectum.
In cases of colorectal DIE, adequate therapy depends on the precise location, extent of the nodule and depth of invasion, as well as the woman's quality of life (3). Removal of the specimen after segmental bowel resection can be performed by either mini-laparotomy (conventional method) or by the natural orifice specimen extraction (NOSE) technique. (8).
The conventional method raises concerns because this could disrupt the integrity of the abdominal wall. Moreover, extraction site laparotomy is associated with higher postoperative pain scores. The occurrence of particular complications such as incisional hernias and wound infections is also higher than after conventional laparoscopic procedures (8).
In order to avoid these complications, NOSE technique has been introduced. During NOSE colectomy the specimen is extracted through a natural orifice and an intracorporeal anastomosis is performed (8).
Several studies have demonstrated a significant drop in pain scores and amelioration of impaired sexual functioning and improved pregnancy rates in women following surgical resection of colorectal endometriosis (9).
The aim of this study is to report the short, medium and long-term bowel functional outcomes and improvement of infertility, quality of life in women undergoing conventional and NOSE segmental bowel resection for endometriosis at our institution using validated questionnaires.
Functional and psychological outcomes will be assessed using different questionnaires at baseline and postoperative follow-up moments.
Endometriosis Health Profile, EHP 30 (10)
Gastrointestinal Quality of Life Index, GIQLI (11)
Low Anterior Resection Syndrome score, LARS (12)
Assessment of endometriosis related pain: Visual Analog Scale (13)
Psychological questionnaires: Pain catastrophizing Scale (14), Self-Efficacy for Managing Chronic Disease 6-item Scale (15).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometriosis, Quality of Life
Keywords
Fertility, Colorectal endometriosis, Surgery
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Our study was designed as a two-arm prospective randomized trial where all cases will be executed unblindly. As an experimental clinical trial the cases have been managed independently where the applied measures were computer based randomization.
In addition clustering effect has been examined within the two groups. The statistical power will be calculated for a sample size.
Randomization: Blinding in our study is not feasible.
Assignment of a patient to conventional or NOSE-colorectal resection is based on a randomization list using the simple randomization method. In order to determine the allocation sequence a computer based (www.random.org) coin flipping is carried out by a staff member with no clinical involvement in the study. The randomization will start after the patient had completed all baseline assessments and had given written consent to be enrolled in the trial.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Patients operated with conventional laparoscopic technique
Arm Type
Active Comparator
Arm Description
Patients operated with conventional laparoscopic technique for colorectal DIE
Arm Title
Patients operated with NOSE laparoscopic technique
Arm Type
Active Comparator
Arm Description
Patients operated with NOSE technique for colorectal DIE
Intervention Type
Procedure
Intervention Name(s)
Surgical procedures( conventional laparoscopic and NOSE technique) for the treatment of colorectal DIE
Intervention Description
For conventional laparoscopic and NOSE techniques a 4-port approach is used. The rectum is skeletonized. The distal rectum is closed using an endoscopic linear stapler. The mobilized rectum with the specimen is retrieved through a small suprapubic incision. The anvil of a conventional circular stapler is introduced in the proximal colon after placement of a purse string suture. A circular stapled colorectal anastomosis is fired. In case of NOSE, both the proximal sigmoid colon and the proximal rectum are tied off laparoscopically with a nonabsorbable suture. A transverse colotomy is performed in healthy tissue using a harmonic scalpel to deliver the anvil from a circular stapler introduced through the anus. The specimen is extracted transrectally in a specimen retrieval bag. Proximal part of the anastomosis is completed by suturing the anvil in place with a laparoscopic suture. The distal rectum is closed using a linear stapler. End-to-end anastomosis is made using the circular stapler
Primary Outcome Measure Information:
Title
Endometriosis Health Profile, EHP 30
Description
To describe the difference in patient reported outcomes after conventional segmental bowel resection treatment in comparison to NOSE colectomy in patients with deep endometriosis infiltrating the rectum.
The patients are asked to fill the questionnaires preoperatively, at 30 days, 6 months, 1 year and 2 years after the surgery. During the present study investigators are planning an average follow-up of 24 months.
Impact of surgical technique on the quality of life. The outcome will be assessed using validated electronic questionnaires containing questions from Endometriosis Health Profile 30. This is a core questionnaire which consists of five scales (pain, control and powerlessness, emotional well-being, social support, and self-image) contains a total of 30 items. (10)
Time Frame
24 months
Title
Gastrointestinal Quality of Life Index, GIQLI
Description
To describe the difference in patient reported outcomes after conventional segmental bowel resection treatment in comparison to NOSE colectomy in patients with deep endometriosis infiltrating the rectum.
The patients are asked to fill the questionnaires preoperatively, at 30 days, 6 months, 1 year and 2 years after the surgery. During the present study investigators are planning an average follow-up of 24 months.
GIQLI is a 36-item patient reported outcomes instrument designed to assess GI-specific health-related quality of life in clinical practice of patients with gastrointestinal disorders. It has five domains (GI symptoms, emotion, physical function, social function and medical treatment) and subscores range from 0-4 while the total score range from 0-144. Higher scores mean better GI health-related quality of life. (11)
Time Frame
24 months
Title
LARS score before and after colorectal resection for DIE
Description
To describe the difference in patient reported outcomes after conventional segmental bowel resection treatment in comparison to NOSE colectomy in patients with deep endometriosis infiltrating the rectum.
The patients are asked to fill the questionnaires preoperatively, at 30 days, 6 months, 1 year and 2 years after the surgery. During the present study investigators are planning an average follow-up of 24 months.
The Low Anterior Resection Syndrome (LARS) is a common complication that occures after colorectal surgery. The LARS score is a simple self-administered questionnaire measuring bowel dysfunction after rectal surgery. Contains questions regarding incontinence, emptying difficulties, urgency, and frequency. The calculated score ranges from 0 to 42, with a score of 0-20 representing no LARS, a score of 21-29 representing minor LARS and a score of 30-42 representing major LARS. (12)
Time Frame
24 months
Title
Endometriosis related pain before and after colorectal resection for DIE
Description
To describe the difference in patient reported outcomes after conventional segmental bowel resection treatment in comparison to NOSE colectomy in patients with deep endometriosis infiltrating the rectum.
The patients are asked to fill the questionnaires preoperatively, at 30 days, 6 months, 1 year and 2 years after the surgery. During the present study investigators are planning an average follow-up of 24 months.
For the assessment of pre- and postoperative pain a Visual Analogue Scale is used (from 1-10, where 1 is the lowest and 10 is the maximum score) to assess the pre- and postoperative quality of life (dysmenorrhoea, dyspareunia, dyschezia, dysuria, CPP) (13).
Time Frame
24 months
Title
Infertility outcomes after colorectal resection for bowel endometriosis
Description
Number of pregnancies, cumulative pregnancy rate and take home baby rate after laparoscopic bowel resection.
Time Frame
24 months
Title
Psychological questionnaires:
Description
To describe the difference in patient reported outcomes after conventional segmental bowel resection treatment in comparison to NOSE colectomy in patients with deep endometriosis infiltrating the rectum.
The patients are asked to fill the questionnaires preoperatively, at 30 days, 6 months, 1 year and 2 years after the surgery. During the present study investigators are planning an average follow-up of 24 months.
Pain catastrophizing Scale, Self-Efficacy for Managing Chronic Disease 6-item Scale to investigate the psychological aspect of the disease (14,15).
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Complication rates after conventional and NOSE-colectomy performed for colorectal endometriosis
Description
To measure the complication rates after conventional and NOSE-colectomy performed for colorectal endometriosis. The complication rates between the NOSE vs conventional specimen extraction technique will be examined. The difference between the complication rates will be presented according to Clavien-Dindo Classification System (16).
As follows:
Grade I Any deviation from the normal postoperative course without treatment by invasive interventions Grade II Requiring pharmacological treatment with drugs other than such allowed for grade I complications.
Grade III
Requiring surgical, endoscopic or radiological intervention
IIIa
Intervention not under general anesthesia
IIIb
Intervention under general anesthesia Grade IV
Life-threatening complication requiring IC/ICU-management
IVa
single organ dysfunction (including dialysis)
IVb
multiorgan dysfunction Grade V Death of a patient
Time Frame
24 months
Title
Hospital stay after colorectal resection perfomed for the treatment of bowel endometriosis
Description
To measure the hospital stay after colorectal resection perfomed for the treatment of bowel endometriosis
Time Frame
24 months
Title
Lenght of recovery after colorectal resection performed for the treatment of bowel endometriosis
Description
To measure the lenght of recovery after bowel resection will be assessed by the comparison of the hospital stay (mean +/- SD days)
Time Frame
24 months
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Hundred and fifty (n=150) premenopausal women with deep infiltrating endometriosis of the rectum who are scheduled for surgical treatment for DIE in our institution during the time will be included in the study.
All women with suspicion of a deep endometriosis will be examined (gynecological examination) by a surgeon experienced in endometriosis. For further mapping of the endometriosis following imaging techniques will be used:
Transvaginal ultrasound using the IDEA terminology to describe the endometriotic lesions found (17)
Complementary examinations can be needed depending on the lesions that are found. For example, MR examination, or intravenous pyelogram in women with associated involvement of the urine tract.
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Age: 18 - 45 years (both inclusive)
Complaining of infertility and/or pain
Deep endometriosis infiltrating the rectum on at least one imaging technique or confirmed by previous surgery
up to 15 cm from the anus
Involving at least the muscularis layer in depth
Exclusion criteria
A potential subject who meets any of the following criteria will be excluded from participation in this study:
Suspected pelvic malignancy
Pregnancy
Patients without bowel resection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Attila Bokor, MD, PhD
Organizational Affiliation
Semmelweis University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Noemi Dobo, MD
Organizational Affiliation
Semmelweis University
Official's Role
Study Chair
Facility Information:
Facility Name
Semmelweis University
City
Budapest
ZIP/Postal Code
1088
Country
Hungary
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Will individual participant data will be available (including datadictionaires)? Individual participant data will be available. What data in particular will be shared? Individual participant data that underline the results reported in the article after deidentification (text, tables, figures and appendices) will be shared.
What other documents will be available? Study protocol, statistical analysis plan, analytic code will be available as well.
When will data be available (start and end dates)? Data will be available from 3 months to 5 years after the publication of the article.
With whom? The data will be shared with researchers who provide a methodologically sound proposal.
For what types of analysis? To achieve aims in the approved proposal. By what mechanism will data be made available? Proposals should be directed to attila.z.bokor@gmail.com. To gain access, data requestors will need to sign a data access agreement. Data are available for 5 years.
IPD Sharing Time Frame
5 years after study closure
IPD Sharing Access Criteria
Any researcher intersted in the study
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The Impact of NOSE-colectomy on Fertility and Quality of Life Among Patients With Colorectal Endometriosis
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