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

Comparison of preoperative bathing effectiveness with three solutions in patients undergoing hip arthroplasty: a clinical study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4hsfyg
Enrollment
Unknown
Registered
2016-05-17
Start date
2015-07-18
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Postoperative infection Surgical Wound Infection

Interventions

Two groups of intervention and a control group consisting of 153 patients undergoing hip arthroplasty, will be randomized to perform preoperative baths with chlorhexidine gluconate solutions to 4%, Po
Procedure/surgery
C01.539.947.692

Sponsors

Universidade Federal de Minas Gerais - UFMG
Lead Sponsor
Universidade Federal de Minas Gerais - UFMG
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
Comparison of demographic factors for groups of patients undergoing interventions: Mean age, sex, BMI, comorbidities. Allergic reactions by types of solutions. Evaluated for changes in the skin or respiratory, during use of the solutions

Countries

Brazil

Contacts

Public ContactFlávia Ercole

Universidade Federal de Minas Gerais - UFMG

flavia.ercole@gmail.com+55 (31) 3409 9176

Outcome results

None listed

Source: REBEC (via WHO ICTRP)