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Does Administration of Antibiotics in Patients Undergoing Surgery for Colorectal Cancer Result in Less Complications and Better Prognosis? (SELECT)

Primary Purpose

Colorectal Cancer

Status
Terminated
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
Selective decontamination of the digestive tract (SDD) (colistin sulfate, tobramycin, amphotericin B)
Sponsored by
H. Jaap Bonjer, PhD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Colorectal Cancer focused on measuring Selective decontamination of the digestive tract, anastomotic leakage, colorectal cancer

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Elective colon and rectal cancer surgery with primary anastomosis
  • Or elective colorectal surgery for suspected carcinoma
  • No evidence of distant metastases (preoperative CT-abdomen and X-thorax or CTthorax)
  • Procedure either with or without diverting stoma
  • Both laparoscopic and open surgery
  • Informed consent
  • Aged 18 years or older

Exclusion Criteria:

  • Previous colorectal malignancy
  • Current malignancy which is now undergoing treatment
  • Inflammatory bowel disease (Crohn's disease or ulcerative colitis)
  • Previous surgery for diverticular disease
  • Performance status ASA 4 or higher (American Society for Anaesthesiologists)
  • Expected adverse reactions/allergies for study medication
  • Prednisone use > 5 mg per day
  • Familial adenomatous polyposis coli (FAP; Lynch syndrome), Hereditary Non Polyposis Colorectal Cancer (HNPCC)
  • Mental disorder/unable to give informed consent
  • Pregnancy

Sites / Locations

  • Slotervaart Ziekenhuis
  • VU University Medical Center
  • Kennemer Gasthuis
  • Spaarne Ziekenhuis
  • WestFries Gasthuis

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard treatment

Selective decontamination of the digestive tract (SDD)

Arm Description

Standard treatment for colorectal cancer

Standard treatment + SDD perioperatively 4 times daily 10 ml of SDD suspension, consisting of 100mg colistin sulfate, 80mg tobramycin and 500mg of amphotericin B. SDD treatment starts 3 days before surgery and is continued until at least 3 days postoperatively.

Outcomes

Primary Outcome Measures

anastomotic leakage and/or abscess
clinical and/or radiological evidence of anastomotic dehiscence requiring surgical or radiological (re)intervention.

Secondary Outcome Measures

Disease free survival

Full Information

First Posted
November 27, 2012
Last Updated
November 7, 2018
Sponsor
H. Jaap Bonjer, PhD
Collaborators
Dutch Digestive Diseases Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01740947
Brief Title
Does Administration of Antibiotics in Patients Undergoing Surgery for Colorectal Cancer Result in Less Complications and Better Prognosis?
Acronym
SELECT
Official Title
Perioperative Selective Decontamination of the Digestive Tract (SDD) in Elective Colorectal Cancer Patients: a Multicenter Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Terminated
Why Stopped
Superiority was no longer attainable
Study Start Date
January 2013 (undefined)
Primary Completion Date
March 2017 (Actual)
Study Completion Date
March 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
H. Jaap Bonjer, PhD
Collaborators
Dutch Digestive Diseases Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary objectives of this randomized clinical trial are to evaluate if perioperative SDD can reduce clinical anastomotic leakage rate and its septic consequences as well as other infectious complications. By reduction of septic complications long-term oncological outcome might simultaneously improve.
Detailed Description
Rationale: Infectious complications and especially anastomotic leakage severely impede the recuperation of patients following colorectal cancer surgery. When the normal gut barrier fails such as in anastomotic leakage, pathogenic microorganisms like Gram-negative bacteria enter the circulation and may cause severe sepsis which is associated with considerable mortality. Moreover, anastomotic leakage has a negative impact on colorectal cancer prognosis. Selective decontamination of the digestive tract (SDD) is a prophylaxis regimen that employs oral nonabsorbable antibiotics to eradicate pathogenic micro-organisms like Gram-negative bacteria. Objective: The primary objectives of this randomized clinical trial are to evaluate if perioperative SDD can reduce clinical anastomotic leakage rate and its septic consequences as well as other infectious complications. By reduction of septic complications long-term oncological outcome might simultaneously improve. Secondary objectives are a decline in reoperation rate, in-hospital mortality, readmission rate, duration of hospital stay and ICU admission, non-infectious complications, improvement of quality of life and reduction of costs. Study design: A randomised multicenter clinical trial comparing perioperative SDD in addition to standard antibiotic prophylaxis with standard antibiotic prophylaxis alone in patients with colorectal cancer who undergo elective surgical resection with curative intent. Study population: Patients 18 years or older are eligible for inclusion when they are diagnosed with colon or rectal cancer without signs of distant metastases. Patients may be scheduled for either laparoscopic or open resection with curative intent, including construction of an anastomosis (either with or without diverting stoma). Patients are not eligible for inclusion in case of concomitant metastases or acute obstruction. Intervention: Patients are randomly allocated for either perioperative SDD (intervention group) including standard antibiotic prophylaxis or standard treatment (including standard antibiotic prophylaxis alone) (control group). The solution containing SDD is orally taken 4 times daily, starting 3 days before surgery and continued until normal bowel passage or at least 3 days after surgery. Both groups receive a single preoperative intravenous dose of 1000 mg Cefazoline and 500 mg Metronidazole, which is the current standard antibiotic prophylaxis. Main study parameters/endpoints: The main study parameter is anastomotic leakage. The research hypothesis refers to an estimated decrease in anastomotic leakage rate in the SDD treated group (from 9% to 4%). As anastomotic leakage has been shown unfavourable forlong term oncological outcome, we presume an improvement in disease free survival, which serves as important secondary endpoint.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Selective decontamination of the digestive tract, anastomotic leakage, colorectal cancer

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
485 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard treatment
Arm Type
No Intervention
Arm Description
Standard treatment for colorectal cancer
Arm Title
Selective decontamination of the digestive tract (SDD)
Arm Type
Experimental
Arm Description
Standard treatment + SDD perioperatively 4 times daily 10 ml of SDD suspension, consisting of 100mg colistin sulfate, 80mg tobramycin and 500mg of amphotericin B. SDD treatment starts 3 days before surgery and is continued until at least 3 days postoperatively.
Intervention Type
Drug
Intervention Name(s)
Selective decontamination of the digestive tract (SDD) (colistin sulfate, tobramycin, amphotericin B)
Other Intervention Name(s)
SDD
Intervention Description
SDD suspension contains per dose of 10 ml 100 mg colistin sulfate, 80 mg tobramycin and 500 mg amphotericin B
Primary Outcome Measure Information:
Title
anastomotic leakage and/or abscess
Description
clinical and/or radiological evidence of anastomotic dehiscence requiring surgical or radiological (re)intervention.
Time Frame
30 days postoperatively
Secondary Outcome Measure Information:
Title
Disease free survival
Time Frame
3 and 5 years after inclusion
Other Pre-specified Outcome Measures:
Title
Other postoperative infectious complications
Description
pneumonia, urinary tract infections, surgical site infections, wound dehiscence, (remote) intraabdominal abscess
Time Frame
30 days postoperatively
Title
Non-infectious complications
Description
cardiac failure, cerebrovascular events, deep venous thrombosis
Time Frame
30 days postoperatively
Title
In-hospital mortality
Time Frame
30 days postoperatively
Title
Readmission rate
Time Frame
5 years postoperatively
Title
Reoperation rate
Time Frame
5 years postoperatively
Title
Duration of hospital stay
Time Frame
30 days postoperatively
Title
Quality of life (quality adjusted life years)
Time Frame
2 years postoperatively
Title
In hospital and out-of-hospital costs
Time Frame
5 years postoperatively

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Elective colon and rectal cancer surgery with primary anastomosis Or elective colorectal surgery for suspected carcinoma No evidence of distant metastases (preoperative CT-abdomen and X-thorax or CTthorax) Procedure either with or without diverting stoma Both laparoscopic and open surgery Informed consent Aged 18 years or older Exclusion Criteria: Previous colorectal malignancy Current malignancy which is now undergoing treatment Inflammatory bowel disease (Crohn's disease or ulcerative colitis) Previous surgery for diverticular disease Performance status ASA 4 or higher (American Society for Anaesthesiologists) Expected adverse reactions/allergies for study medication Prednisone use > 5 mg per day Familial adenomatous polyposis coli (FAP; Lynch syndrome), Hereditary Non Polyposis Colorectal Cancer (HNPCC) Mental disorder/unable to give informed consent Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
H.J. Bonjer, Md, PhD, FRCSC
Organizational Affiliation
Amsterdam UMC, location VUmc
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
G.S.A. Abis, MD, MSc
Organizational Affiliation
Amsterdam UMC, location VUmc
Official's Role
Study Director
Facility Information:
Facility Name
Slotervaart Ziekenhuis
City
Amsterdam
Country
Netherlands
Facility Name
VU University Medical Center
City
Amsterdam
Country
Netherlands
Facility Name
Kennemer Gasthuis
City
Haarlem
Country
Netherlands
Facility Name
Spaarne Ziekenhuis
City
Hoofddorp
Country
Netherlands
Facility Name
WestFries Gasthuis
City
Hoorn
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
30802304
Citation
Abis GSA, Stockmann HBAC, Bonjer HJ, van Veenendaal N, van Doorn-Schepens MLM, Budding AE, Wilschut JA, van Egmond M, Oosterling SJ; SELECT trial study group. Randomized clinical trial of selective decontamination of the digestive tract in elective colorectal cancer surgery (SELECT trial). Br J Surg. 2019 Mar;106(4):355-363. doi: 10.1002/bjs.11117. Epub 2019 Feb 25.
Results Reference
derived
PubMed Identifier
24814583
Citation
Abis GS, Oosterling SJ, Stockmann HB, van der Bij GJ, van Egmond M, Vandenbroucke-Grauls CM, Bonjer HJ. Perioperative selective decontamination of the digestive tract and standard antibiotic prophylaxis versus standard antibiotic prophylaxis alone in elective colorectal cancer patients. Dan Med J. 2014 Apr;61(4):A4695.
Results Reference
derived

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Does Administration of Antibiotics in Patients Undergoing Surgery for Colorectal Cancer Result in Less Complications and Better Prognosis?

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