Skip to content

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

Perioperative Selective Decontamination of the Digestive Tract (SDD) in Elective Colorectal Cancer Patients: a Multicenter Randomized Clinical Trial

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01740947
Acronym
SELECT
Enrollment
485
Registered
2012-12-04
Start date
2013-01-31
Completion date
2017-03-31
Last updated
2018-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer

Keywords

Selective decontamination of the digestive tract, anastomotic leakage, colorectal cancer

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.

Interventions

DRUGSelective decontamination of the digestive tract (SDD) (colistin sulfate, tobramycin, amphotericin B)

SDD suspension contains per dose of 10 ml 100 mg colistin sulfate, 80 mg tobramycin and 500 mg amphotericin B

Sponsors

Dutch Digestive Diseases Foundation
CollaboratorOTHER
H. Jaap Bonjer, PhD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
anastomotic leakage and/or abscess30 days postoperativelyclinical and/or radiological evidence of anastomotic dehiscence requiring surgical or radiological (re)intervention.

Secondary

MeasureTime frame
Disease free survival3 and 5 years after inclusion

Other

MeasureTime frameDescription
In-hospital mortality30 days postoperatively
Readmission rate5 years postoperatively
Reoperation rate5 years postoperatively
Other postoperative infectious complications30 days postoperativelypneumonia, urinary tract infections, surgical site infections, wound dehiscence, (remote) intraabdominal abscess
Quality of life (quality adjusted life years)2 years postoperatively
In hospital and out-of-hospital costs5 years postoperatively
Duration of hospital stay30 days postoperatively
Non-infectious complications30 days postoperativelycardiac failure, cerebrovascular events, deep venous thrombosis

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026