Hospital-acquired bloodstream infections. Bacterial infection, unspecified
Conditions
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Confirmation of the occurrence of sepsis in patients with the initial assessment of the patient's clinical symptoms and laboratory parameters Patients over 18 years old Primary diagnosis of sepsis (have at least two of the following four symptoms: hypothermia or hyperthermia, tachycardia, tachypnea, and leukocytosis or leukopenia) by an infectious specialist or a positive MDR culture
Exclusion criteria
Exclusion criteria: History of consuming corticosteroids and immunosuppressive drugs Pregnant and lactating mothers
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measurement of inflammatory factors. Timepoint: Measurement at the beginning of the study (before the start of the intervention) and 14 days after the start of NBS powder consumption. Method of measurement: Gold standard methods (ESR measurement by Westergren method, CRP measurement by Electrochemical Immunoassay method).;Measurement of white blood cells. Timepoint: Measurement at the beginning of the study (before the start of the intervention) and 14 days after the start of NBS powder consumption. Method of measurement: Cell Counter. | — |
Secondary
| Measure | Time frame |
|---|---|
| Mortality Rate. Timepoint: After completing the intervention. Method of measurement: Checking the patient's clinical symptoms. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMehrdad Mosadegh
Tehran University of Medical Sciences
Outcome results
None listed