Assessment of the incidence of surgical site infections after surgery for colorectal cancer with preoperative oral antibiotics.

Not Applicable

• Conditions: Patients with surgery forcolorectal cancer

• Registration Number: JPRN-UMIN000037301
• Lead Sponsor: Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-07-15
• Study Completion: 2020-12-01
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

Not provided

Exclusion Criteria

Patients with allergy for Ciprofloxacin and Metronidazole. Patients who have difficulty with oral administration due to intestinal obstruction.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The rate of surgical site infection at 30th days after surgery

Secondary Outcome Measures

Name	Time	Method
Safety of the preoperative oral antibiotics and, Incidence of postoperative suture failure, incidence of postoperative ileus, incidence of urinary tract infection