Sepsis. Other sepsis
Conditions
Interventions
Intervention 1: Control group: Control group: All selected patients will be treated for sepsis based on standard guideline recommendations. According to these guidelines, 30 mL/kg of lactated Ringer's
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with sepsis hospitalized in the intensive care unit
Exclusion criteria
Exclusion criteria: Inaccessible peripheral perfusion
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Prevalence of peripheral hypoperfusion among the study groups. Timepoint: Every 30 seconds for 5 minutes daily over a span of seven days. Method of measurement: Pulse oximeter. | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood lactate level. Timepoint: Between 6 and 24 hours after sepsis diagnosis. Method of measurement: Blood sample.;Mean arterial pressure. Timepoint: Between 6 and 24 hours after sepsis diagnosis. Method of measurement: Intensive care monitoring device.;Serum cystatin C level. Timepoint: Between 6 and 24 hours after sepsis diagnosis. Method of measurement: Blood sample. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSara Mousavi
Esfahan University of Medical Sciences
Outcome results
None listed