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Triclosan-coated sutures versus uncoated sutures for prevention of surgical site infection after abdominal wall closure in open/laparoscopic colorectal surgery

Not Applicable
Conditions
Surgical site infection
Registration Number
JPRN-UMIN000042605
Lead Sponsor
Multicenter Clinical Study Group of Osaka, Colorectal Cancer Treatment Group
Brief Summary

The recorded SSI rates were 4.2% in the triclosan-coated group and 6.74% in the uncoated suture group (p = 0.028). There were no serious adverse events in the groups. The final logistic regression model showed that several variables affected the occurrence of SSI. Our meta-analysis included six phase-III trials, and our study evaluated 4,797 patients. The results show a significant superiority of triclosan-coated sutures over uncoated suture material.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
2207
Inclusion Criteria

Not provided

Exclusion Criteria

1) There is no history of surgical wounds on the planned surgical site. 2) Do not perform surgery on other organs in different locations at the same time. 3) No history of radiation therapy or chemotherapy. 4) No contamination or infection surgery.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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