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Comparison of effect of bath performed before hip prosthesis surgery with three different solutions

Not Applicable
Recruiting
Conditions
Postoperative infectionSurgical Wound Infection
C01.539.947.692
Registration Number
RBR-4hsfyg
Lead Sponsor
niversidade Federal de Minas Gerais - UFMG
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Patient with an elective procedure of total hip arthroplasty; age of 18 years or more; no report of infection at the surgical site; with access to landline or mobile; know autodiagnosticar informing the clinical signs of the infection or have a responsible with this ability; don't be Staphylococcus aureus nasal carrier prior to surgery.

Exclusion Criteria

Patient treatment of surgical site infection; undergoing hip replacement surgery in urgency situations; emergency; orthopedic trauma; with a history of allergic reactions to the products used in the bath; underwent partial hip arthroplasty surgery; nasal Staphylococcus aureus carriers before surgery.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Presence or absence of Surgical Site Infection (SSI) in patients undergoing hip arthroplasty who used one of the three solutions (chlorhexidine gluconate 4%, 10% povidone and soap without antiseptic). The diagnosis of ISC will be performed using the diagnostic criteria Surgical Site Infection of the National Healthcare Safety Network/Centers for Disease Control and Prevention- NHSN/CDC. For the detection of ISC patients will be followed up by phone calls during the period of 30, 60 and 90 days or doctor's office. In the analysis of infections the SSI incidence rates for each intervention for comparison. To determine whether associations found and differences are statistically significant will use the 5% significance leve.
Secondary Outcome Measures
NameTimeMethod
Comparison of demographic factors for groups of patients undergoing interventions: Mean age, sex, BMI, comorbidities.<br>Allergic reactions by types of solutions. Evaluated for changes in the skin or respiratory, during use of the solutions<br>
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