Mechanical Bowel Preparation Versus no Bowel Preparation for Esophageal Cancer Surgery
Primary Purpose
Esophageal Cancer
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
No MBP
Sponsored by
About this trial
This is an interventional treatment trial for Esophageal Cancer
Eligibility Criteria
Inclusion Criteria:
- Patients who were scheduled for esophageal cancer resection in participating centers were eligible for inclusion.
Exclusion Criteria:
- need for emergency surgery;
- previous chronic constipation or diarrhea;
- previous abdominal surgery; need for colonic reconstruction;
- other indications for mechanical preparation or contraindications;
- allergy to drugs used in the trial (polyethylene glycol)
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
NBP group
MBP group
Arm Description
Patients allocated to NBP were instructed to not prepare the bowel.
Patients allocated to MBP were instructed by the study nurse to prepare their bowel mechanically by drinking 3~4L of polyethylene glycol (Polyethylene Glycol Electrolytes Powder 68.56g; Shenzhen, China) with water before 6pm in the evening the day before the surgery.
Outcomes
Primary Outcome Measures
the rate of major complications
A major intraoperative and postoperative complication was defined as a surgical or medical complication with a Clavien-Dindo (CD) grade of Ⅱor higher (this five-grade system includes sub-grades in grades Ⅲ and Ⅳ, and higher grades indicate more life-threatening complications) according to Esophagectomy Complications Consensus Group (ECCG)
Secondary Outcome Measures
Full Information
NCT ID
NCT05523960
First Posted
August 29, 2022
Last Updated
August 29, 2022
Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
1. Study Identification
Unique Protocol Identification Number
NCT05523960
Brief Title
Mechanical Bowel Preparation Versus no Bowel Preparation for Esophageal Cancer Surgery
Official Title
Mechanical Bowel Preparation Versus no Bowel Preparation for Esophageal Cancer Surgery: a Multi-center, Randomized, Parallel, Single-blinded Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2022 (Anticipated)
Primary Completion Date
January 1, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
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
The study type was designed as a prospective multicenter randomized controlled study. The patients will be divided into intervention group (126 cases) and control group, 281 patients were needed for each group and 562 patients would be needed totally to show this difference. The intervention group will not implement mechanical bowel preparation(MBP) before surgery; the control group will receive routine preoperative MBP for oral administration of compound polyethylene glycol electrolyte powder and fasting water. Perioperative complications, intestinal recovery speed and quality of life will be investigated between the two groups.
Detailed Description
Patients allocated to MBP will be instructed by the study nurse to prepare their bowel mechanically by drinking 3~4L of polyethylene glycol (Polyethylene Glycol Electrolytes Powder 68.56g; Shenzhen, China) with water before 6pm in the evening the day before the surgery. Patients allocated to NBP were instructed to not prepare the bowel. The receipt of the allocated intervention will be controlled by study nurse asking the patients on the morning of the surgery whether they had acted as instructed by the allocation. This information will be also concealed from treating physicians and surgeons, data collectors, and data analysts, until the primary and secondary outcomes were analyzed. All patients will follow the ERAS protocol. Prophylactic intravenous antibiotics (cephamycin 1000mg) will be given to all patients 30 minutes before skin incision. The prophylactic intravenous antibiotics will re-administered if the surgery lasted longer than 3h from the first antibiotic dose. Surgical skin preparation will involve taking a bath well the night before operation without shaving the hair. Just before skin incision, the area will then washed three times with denatured 80% alcohol to left to dry.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
562 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
NBP group
Arm Type
Experimental
Arm Description
Patients allocated to NBP were instructed to not prepare the bowel.
Arm Title
MBP group
Arm Type
Other
Arm Description
Patients allocated to MBP were instructed by the study nurse to prepare their bowel mechanically by drinking 3~4L of polyethylene glycol (Polyethylene Glycol Electrolytes Powder 68.56g; Shenzhen, China) with water before 6pm in the evening the day before the surgery.
Intervention Type
Procedure
Intervention Name(s)
No MBP
Intervention Description
No mechanical bowel preparation before operation
Primary Outcome Measure Information:
Title
the rate of major complications
Description
A major intraoperative and postoperative complication was defined as a surgical or medical complication with a Clavien-Dindo (CD) grade of Ⅱor higher (this five-grade system includes sub-grades in grades Ⅲ and Ⅳ, and higher grades indicate more life-threatening complications) according to Esophagectomy Complications Consensus Group (ECCG)
Time Frame
during surgery orwithin 30 days after surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients who were scheduled for esophageal cancer resection in participating centers were eligible for inclusion.
Exclusion Criteria:
need for emergency surgery;
previous chronic constipation or diarrhea;
previous abdominal surgery; need for colonic reconstruction;
other indications for mechanical preparation or contraindications;
allergy to drugs used in the trial (polyethylene glycol)
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Mechanical Bowel Preparation Versus no Bowel Preparation for Esophageal Cancer Surgery
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