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The Effect of Mechanical Bowel Preparation Prior to Gynaecological Laparoscopic Surgeries on the Surgical Conditions

Primary Purpose

Patient Preference, Patient Safety

Status
Unknown status
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Mechanical Bowel Preparation
Low fibre diet
MBP plus low-fibre diet
Sponsored by
Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Patient Preference focused on measuring mechanical bowel preparation, gynecological surgery, Minimally invasive gynecological procedures, Enema, Trendelenburg angle, Pneumoperitoneum pressure

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Aged 18 years and older
  • Able to provide informed consent
  • Undergo laparoscopic gynecological surgery for a benign condition

Exclusion Criteria:

  • History of previous abdominal surgery
  • Clinically significant present or past systemic diseases
  • Inability to perform mechanical bowel preparation
  • Suspicion of malignancy
  • Association with non-gynaecological surgical pathologies
  • Severe endometriosis (stage ≥ III according to the classification of the American Society for Reproductive Medicine)
  • Psychiatric disorders precluding consent

Sites / Locations

  • Egemed HospitalRecruiting
  • Samsun Medical FacultyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Active Comparator

No Intervention

Arm Label

Mechanical Bowel Preparation

Low fibre diet

MBP plus low fibre diet

Control

Arm Description

Patients will have only clear liquids after a normal breakfast and lunch on the day before surgery and subsequently fasten for 7-9 hours prior to surgery. Patients will ingest first dose of 45 ml oral sodium phosphate (NaP) enema (BT ORAL SOLUSYON 45 ML®, Yenisehir Lab. Tic. San. Ltd. Sti, Turkey) at 4 p.m. and a second dose at 8 p.m. in the evening before the scheduled surgery.

Patients will be given detailed instructions about the pre-operative diet (total daily Fibre intake inferior to 10 g) to be used for 3 days prior to surgery.

This group will receive both mechanical bowel preparation and 3-days low fibre diet.

Control subjects will receive no instructions about the pre-operative diet (free diet).

Outcomes

Primary Outcome Measures

The surgical visibility of abdomen
A scale title as "Objective Visual Indexing (OVI)" will be used for assessing the visibility of the Douglas pouch and adnexa. The assessment of the visibility of Douglas pouch and adnexa will be performed under standard pneumoperitoneum pressure (12mmHg) and Trendelenburg inclincation angle (30). After the first Inspection, scale of VI scoring will be calculated by adding up the points obtained from optical inspection. Higher scores mean better visuality of the surgical field.
The lowest pneumoperitoneum pressure (PP) at standard Trendelenburg inclination angle (TIA).
The PP will be increased to 15 mmHg while keeping the TIA same, at 30o. The surgeon will displace the bowel beginning from the cecum followed by the last ileal loop above the sacral promontory. Once the bowel was displaced out of the pelvis, the PP will be stepwise decreased by 1 mmHg during 1 min intervals to the lowest pressure where the bowel is to descend towards the pelvis over the pelvic brim and/or where the surgical workspace is not adequate to proceed safely with the planned operation. This value will be recorded as the lowest PP adequate to proceed safely with the planned surgery at standard TIA (30 degree).
The lowest Trendelenburg inclination angle (TIA) at standard pneumoperitoneum pressure (PP) adequate to proceed with the planned operation.
The PP obtained in outcome 2 will be readjusted to the standard 12 mmHg keeping the TIA same, at 300. Then, the surgeon will replace the bowel beginning from the cecum followed by the last ileal loop above the sacral promontory. Once the bowel is displaced out of the pelvis, the TIA will be gradually decreased by 1o with 15 seconds intervals to the degree where the bowel is to descend towards the pelvis over the pelvic brim. This value will be recorded as the lowest TIA adequate to proceed safely with the planned surgery at standard PP (12 mmHg).

Secondary Outcome Measures

Preoperative patient symptomatology
Patients will be interviewed in the preoperative holding area or in the patient's room about the acceptability of the intervention (MBP / diet) and adverse pre-operative events, including: nausea, insomnia, headache, thirst, weakness, tiredness, discomfort, abdominal cramps, sleep disturbances. These symptoms will be scored with using a 10-cm "Visual Analog Score" (VAS). Higher scores mean worse outcome.
Postoperative pain
The intensity of the postoperative pain was measured by an independent investigator at 24th hours with a 10-cm Visual Analog Score (VAS). Higher scores mean worse outcome.
Complications
Intraoperative complications, at 1st week and 6th week postoperatively, between the groups.

Full Information

First Posted
May 19, 2020
Last Updated
February 11, 2021
Sponsor
Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital
Collaborators
Ondokuz Mayıs University
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1. Study Identification

Unique Protocol Identification Number
NCT04400669
Brief Title
The Effect of Mechanical Bowel Preparation Prior to Gynaecological Laparoscopic Surgeries on the Surgical Conditions
Official Title
The Effect of Mechanical Bowel Preparation Prior to Gynaecological Laparoscopic Surgeries on the Pressure of Pneumoperitoneum and Trendelenburg Inclination Angle During the Surgery: A Novel Perspective for Patient Safety
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 5, 2020 (Actual)
Primary Completion Date
November 5, 2021 (Anticipated)
Study Completion Date
November 20, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research Hospital
Collaborators
Ondokuz Mayıs 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
This RCT aims to investigate the real surgical effects of MBP prior to the gynecological laparoscopic surgeries. Those effects include lowest pneumoperitoneum pressure, lowest Trendelenburg inclination angle, the ease of the surgical view and the preferences of the patients with objective measures.
Detailed Description
Mechanical bowel preparation (MBP) has been routinely used prior to minimally invasive gynaecologic procedures (MIGP) hypothetically to improve intraoperative bowel handling and visualization of the surgical field, and also to reduce faecal contamination in the setting of bowel injury and/or resection. The studies investigating the effect of MBP on MIGP are limited and most of existing data are extrapolated from the reports of colorectal and urological surgery studies. Besides, evaluation of the surgical workspace visualization and intraoperative bowel handling are far from being objective since they were mostly measured by a 4/5/10-point Likert scales or rated verbally on scales of excellent to poor by the operating surgeons. In contrary, it is planned to use objective visualize index, and objective surgical conditions to measure whether MBP has any effect or not.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Patient Preference, Patient Safety
Keywords
mechanical bowel preparation, gynecological surgery, Minimally invasive gynecological procedures, Enema, Trendelenburg angle, Pneumoperitoneum pressure

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Masking Description
Surgeons and the assessor will be blind. The nurse working in the gynecology setting perform the intervention to the previously randomized patients. Patient will be told for not to reveal the intervention that she undergoes.
Allocation
Randomized
Enrollment
160 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Mechanical Bowel Preparation
Arm Type
Experimental
Arm Description
Patients will have only clear liquids after a normal breakfast and lunch on the day before surgery and subsequently fasten for 7-9 hours prior to surgery. Patients will ingest first dose of 45 ml oral sodium phosphate (NaP) enema (BT ORAL SOLUSYON 45 ML®, Yenisehir Lab. Tic. San. Ltd. Sti, Turkey) at 4 p.m. and a second dose at 8 p.m. in the evening before the scheduled surgery.
Arm Title
Low fibre diet
Arm Type
Active Comparator
Arm Description
Patients will be given detailed instructions about the pre-operative diet (total daily Fibre intake inferior to 10 g) to be used for 3 days prior to surgery.
Arm Title
MBP plus low fibre diet
Arm Type
Active Comparator
Arm Description
This group will receive both mechanical bowel preparation and 3-days low fibre diet.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Control subjects will receive no instructions about the pre-operative diet (free diet).
Intervention Type
Other
Intervention Name(s)
Mechanical Bowel Preparation
Intervention Description
oral sodium phosphate (NaP) enema
Intervention Type
Dietary Supplement
Intervention Name(s)
Low fibre diet
Intervention Description
3 days
Intervention Type
Other
Intervention Name(s)
MBP plus low-fibre diet
Intervention Description
3 days low fibre diet preoperative mechanical bowel preparation
Primary Outcome Measure Information:
Title
The surgical visibility of abdomen
Description
A scale title as "Objective Visual Indexing (OVI)" will be used for assessing the visibility of the Douglas pouch and adnexa. The assessment of the visibility of Douglas pouch and adnexa will be performed under standard pneumoperitoneum pressure (12mmHg) and Trendelenburg inclincation angle (30). After the first Inspection, scale of VI scoring will be calculated by adding up the points obtained from optical inspection. Higher scores mean better visuality of the surgical field.
Time Frame
After the introduce of first left lateral port
Title
The lowest pneumoperitoneum pressure (PP) at standard Trendelenburg inclination angle (TIA).
Description
The PP will be increased to 15 mmHg while keeping the TIA same, at 30o. The surgeon will displace the bowel beginning from the cecum followed by the last ileal loop above the sacral promontory. Once the bowel was displaced out of the pelvis, the PP will be stepwise decreased by 1 mmHg during 1 min intervals to the lowest pressure where the bowel is to descend towards the pelvis over the pelvic brim and/or where the surgical workspace is not adequate to proceed safely with the planned operation. This value will be recorded as the lowest PP adequate to proceed safely with the planned surgery at standard TIA (30 degree).
Time Frame
In the initial phase of the surgery
Title
The lowest Trendelenburg inclination angle (TIA) at standard pneumoperitoneum pressure (PP) adequate to proceed with the planned operation.
Description
The PP obtained in outcome 2 will be readjusted to the standard 12 mmHg keeping the TIA same, at 300. Then, the surgeon will replace the bowel beginning from the cecum followed by the last ileal loop above the sacral promontory. Once the bowel is displaced out of the pelvis, the TIA will be gradually decreased by 1o with 15 seconds intervals to the degree where the bowel is to descend towards the pelvis over the pelvic brim. This value will be recorded as the lowest TIA adequate to proceed safely with the planned surgery at standard PP (12 mmHg).
Time Frame
In the initial phase of the surgery
Secondary Outcome Measure Information:
Title
Preoperative patient symptomatology
Description
Patients will be interviewed in the preoperative holding area or in the patient's room about the acceptability of the intervention (MBP / diet) and adverse pre-operative events, including: nausea, insomnia, headache, thirst, weakness, tiredness, discomfort, abdominal cramps, sleep disturbances. These symptoms will be scored with using a 10-cm "Visual Analog Score" (VAS). Higher scores mean worse outcome.
Time Frame
Right before the surgery
Title
Postoperative pain
Description
The intensity of the postoperative pain was measured by an independent investigator at 24th hours with a 10-cm Visual Analog Score (VAS). Higher scores mean worse outcome.
Time Frame
at 24th hours
Title
Complications
Description
Intraoperative complications, at 1st week and 6th week postoperatively, between the groups.
Time Frame
At 1st week and 6th week postoperatively or whenever it occurred.

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Aged 18 years and older Able to provide informed consent Undergo laparoscopic gynecological surgery for a benign condition Exclusion Criteria: History of previous abdominal surgery Clinically significant present or past systemic diseases Inability to perform mechanical bowel preparation Suspicion of malignancy Association with non-gynaecological surgical pathologies Severe endometriosis (stage ≥ III according to the classification of the American Society for Reproductive Medicine) Psychiatric disorders precluding consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Uzeyir Kalkan, M.D.
Phone
+905428102539
Email
uzekal@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kadir Bakay, Assoc Prof
Organizational Affiliation
Ondokuz Mayis Universitesi
Official's Role
Principal Investigator
Facility Information:
Facility Name
Egemed Hospital
City
Aydin
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Uzeyir Kalkan, M.D.
First Name & Middle Initial & Last Name & Degree
Uzeyir Kalkan, M.D.
Facility Name
Samsun Medical Faculty
City
Samsun
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kadir Bakay, Assoc.Prof.
First Name & Middle Initial & Last Name & Degree
Kadir Bakay, Assoc.Prof.

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Raw data (for meta-analysis), statistical analyses and study protocol can be shared upon request. Processed data can be shared after completion of the study.
IPD Sharing Time Frame
After the completion of the study, for 10 years.
IPD Sharing Access Criteria
Access will be granted right after establishing a contact.
IPD Sharing URL
https://drive.google.com/file/d/1E5qV7Ff_ltsXFYc0m4MgO2a4N-BmVRSQ/view?usp=sharing
Citations:
PubMed Identifier
28650683
Citation
Bakay K, Aytekin F. Mechanical bowel preparation for laparoscopic hysterectomy, is it really necessary? J Obstet Gynaecol. 2017 Nov;37(8):1032-1035. doi: 10.1080/01443615.2017.1318268. Epub 2017 Jun 26.
Results Reference
result

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The Effect of Mechanical Bowel Preparation Prior to Gynaecological Laparoscopic Surgeries on the Surgical Conditions

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