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Mechanical Bowel Preparation With or Without Oral Antibiotics for Colorectal Cancer Surgery (MECCA)

Primary Purpose

Antibiotic, Bowel Cancer, Colorectal Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
Bowel Preparation plus antibiotics
Bowel Preparation
Sponsored by
National and Kapodistrian University of Athens
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Antibiotic focused on measuring oral antibiotic, mechanical bowel preparation, colorectal cancer, surgical site infection

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Scheduled colorectal cancer surgery

Exclusion Criteria:

  • Emergency surgery
  • Obstructive and perforated cancer
  • Intolerance to bowel preparation regimen
  • Allergies to orally administered antibiotics

Sites / Locations

  • NKUAthensRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

Bowel Preparation plus antibiotics

Bowel Preparation

Arm Description

Preoperative oral antibiotic therapy with rifaximin 400 mg plus metronidazole 500mg the day prior to surgery at 2:00, 3:00 and 10:00 pm, with mechanical bowel preparation (2 vials sodium phospate 45ml at 1:00 and 7:00 pm)

Preoperative mechanical bowel preparation (2 vials sodium phospate 45ml at 1:00 and 7:00 pm)

Outcomes

Primary Outcome Measures

Surgical Site Infections
Surgical Site Infections

Secondary Outcome Measures

Anastomotic leaks
Anastomotic leaks
Other surgical and non-surgical compliactions
Other surgical and non-surgical compliactions
Hospital length of stay
Hospital length of stay
Readmission rate
Readmission rate
Patients' preparation tolerance
Patients' preparation tolerance
Preparation regimens side-effects
Preparation regimens side-effects
Time to beginning of adjuvant treatment for colorectal cancer
Time to beginning of adjuvant treatment for colorectal cancer

Full Information

First Posted
June 9, 2018
Last Updated
September 10, 2020
Sponsor
National and Kapodistrian University of Athens
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1. Study Identification

Unique Protocol Identification Number
NCT03563586
Brief Title
Mechanical Bowel Preparation With or Without Oral Antibiotics for Colorectal Cancer Surgery
Acronym
MECCA
Official Title
Prospective Randomized Monocentric Trial of Mechanical Bowel Preparation Alone vs Mechanical Bowel Preparation Combined With Oral Antibiotics Before Colorectal Resections for Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Unknown status
Study Start Date
April 1, 2018 (Actual)
Primary Completion Date
April 1, 2021 (Anticipated)
Study Completion Date
June 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National and Kapodistrian University of Athens

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Investigation of the role of adding oral antibiotics to preoperative mechanical bowel preparation before colorectal surgery for cancer.
Detailed Description
The aim of the study is to investigate whether the addition of oral antibiotics to Mechanical Bowel Preparation (MBP) prior to colorectal cancer surgical procedures reduce the superfical and deep surgical site (SSI) infectious complications. The study is prospective and is designed in a randomized single-blinded controlled fashion. It is taking place at one academic surgical unit of Athens Medical School, located at a tertiary referal institution. Patients scheduled to undergo an elective surgical resection for colon or rectal cancer will be allocated to either formal MBP the day before surgery or a combined MBP with administration of oral antibiotics. Exclusion criteria are the following: emergency surgery, obstructive or perforated cancer, patients intolerance to bowel preparation regimen and allergies to orally administered antibiotics. Intervention arms: Patients will be randomised into two groups, concealed from the treating surgeon. Group A: Preoperative oral antibiotic therapy with rifaximin 400 mg plus metronidazole 500mg the day prior to surgery at 2:00, 3:00 and 10:00 pm, with MBP (2 vials sodium phospate 45ml at 1:00 and 7:00 pm) Group B: MBP (2 vials sodium phospate 45ml at 1:00 and 7:00 pm) alone Both groups will receive iv antibiotics (cefoxitin 2 gr plus metronidazole 500gr) perioperatively and discontinuation within 24 hours. Outcome measures: The primary end point is surgical site infection (SSI), including (i) superficial wound infection, (ii) deep wound infection, and (iii) intrabdominal infection (contaminated fluid or pus collection) within 30 days of the procedure (decrease 3% in the rate) Secondary measures: Anastomotic leaks, other surgical and non-surgical compliactions, hospital length of stay, readmission rate, patients' preparation tolerance, preparation regimens side-effects, time to beginning of adjuvant treatment for colorectal cancer. Sample Size: It is estimated that 105 patients per treatment arm are needed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Antibiotic, Bowel Cancer, Colorectal Cancer, Surgical Site Infection
Keywords
oral antibiotic, mechanical bowel preparation, colorectal cancer, surgical site infection

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Masking
Care ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
210 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Bowel Preparation plus antibiotics
Arm Type
Active Comparator
Arm Description
Preoperative oral antibiotic therapy with rifaximin 400 mg plus metronidazole 500mg the day prior to surgery at 2:00, 3:00 and 10:00 pm, with mechanical bowel preparation (2 vials sodium phospate 45ml at 1:00 and 7:00 pm)
Arm Title
Bowel Preparation
Arm Type
Other
Arm Description
Preoperative mechanical bowel preparation (2 vials sodium phospate 45ml at 1:00 and 7:00 pm)
Intervention Type
Other
Intervention Name(s)
Bowel Preparation plus antibiotics
Intervention Description
Preoperative oral antibiotic therapy with rifaximin 400 mg plus metronidazole 500mg the day prior to surgery at 2:00, 3:00 and 10:00 pm, with mechanical bowel preparation (2 vials sodium phospate 45ml at 1:00 and 7:00 pm)
Intervention Type
Other
Intervention Name(s)
Bowel Preparation
Intervention Description
Mechanical Bowel Preparation (2 vials sodium phospate 45ml at 1:00 and 7:00 pm) alone Both groups will receive iv antibiotics (cefoxitin 2 gr plus metronidazole 500gr) perioperatively and discontinuation within 24 hours
Primary Outcome Measure Information:
Title
Surgical Site Infections
Description
Surgical Site Infections
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Anastomotic leaks
Description
Anastomotic leaks
Time Frame
30 days
Title
Other surgical and non-surgical compliactions
Description
Other surgical and non-surgical compliactions
Time Frame
30 days
Title
Hospital length of stay
Description
Hospital length of stay
Time Frame
30 days
Title
Readmission rate
Description
Readmission rate
Time Frame
30 days
Title
Patients' preparation tolerance
Description
Patients' preparation tolerance
Time Frame
30 days
Title
Preparation regimens side-effects
Description
Preparation regimens side-effects
Time Frame
30 days
Title
Time to beginning of adjuvant treatment for colorectal cancer
Description
Time to beginning of adjuvant treatment for colorectal cancer
Time Frame
60 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Scheduled colorectal cancer surgery Exclusion Criteria: Emergency surgery Obstructive and perforated cancer Intolerance to bowel preparation regimen Allergies to orally administered antibiotics
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
George Theodoropoulos
Phone
+306945463593
Email
georgetheocrs@live.com
First Name & Middle Initial & Last Name or Official Title & Degree
Georgia Georgiou
Phone
+306945292510
Email
georgia_cy@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
George Theodoropoulos
Organizational Affiliation
National and Kapodistrian University of Athens
Official's Role
Principal Investigator
Facility Information:
Facility Name
NKUAthens
City
Athens
ZIP/Postal Code
11528
Country
Greece
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
George Theodoropoulos
Phone
6945463593

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Mechanical Bowel Preparation With or Without Oral Antibiotics for Colorectal Cancer Surgery

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