Surgical Wound Infection
Conditions
Interventions
This is a randomized, controlled, two-arm, single-blind clinical study. A total of 148 patients were included. 71 patients were randomized to the 2% aqueous chlorhexidine intervention group and 77 pat
Sponsors
Irmandade da Santa Casa de Misericordia de Curitiba
Irmandade da Santa Casa de Misericordia de Curitiba
Eligibility
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Paciente who have undergone open bariatric bypass surgery; patients >= 18 years old and <=65 years old; both sexes (female and male)
Exclusion criteria
Exclusion criteria: Patients allergic to chlorhexidine; videolaparoscopic bariatric surgery; sleeve gastrectomy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Our primary outcome was the surgical wound infection rate, and we expected to find a decrease with the use of 2% aqueous chlorhexidine. However, similar rates of surgical wound infection were observed in both groups. 22 patients presented with superficial surgical wound infection in the chlorhexidine group (30.9%) and 19 patients presented with surgical wound infection in the saline group (24.7%), with only one infection classified as deep, requiring surgical intervention in this group. Based on Pearson's chi-square test, no statistically significant difference was observed between the groups, with a p-value of 0.501. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected | — |
Countries
Brazil
Contacts
Public ContactOdair Neto
Hospital Santa Casa de Curitiba
Outcome results
None listed