nosocomial infection. Other and unspecified infectious diseases
Conditions
Interventions
Intervention 1: In the control group, sampling will be done using a sterile swab from areas of the armpits, groin, and neck folds on arrival at the hospital and 48 hours after hospitalization without
Prevention
In the control group, sampling will be done using a sterile swab from areas of the armpits, groin, and neck folds on arrival at the hospital and 48 hours after hospitalization without any intervention
Sampling of the same body areas in the intervention group will be conducted with the same method on arrival at the hospital and 48 hours after hospitalization and daily 2% chlorhexidine bath. For bath
Sponsors
Zahedan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: In these patients, patients with multiple trauma, aged 20-60 who were hospitalized in the ICU for at least 48 hours were selected as the sample. Exclusion criteria: The exclusion criteria were affliction with infectious diseases or diabetes, pregnancy (for women), and discharge or transfer to another ward before 48 hours.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Colonies number. Timepoint: First and third days of hospitalization. Method of measurement: culture.;Type of micro-organisms. Timepoint: First and third days of hospitalization. Method of measurement: culture.;Drug resistance. Timepoint: First and third days of hospitalization. Method of measurement: Antibiotic SensitivityTest. | — |
Secondary
| Measure | Time frame |
|---|---|
| Duration of hospitalization. Timepoint: -. Method of measurement: days. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHamed sarani
Zahedan University of Medical Sciences
Outcome results
None listed