Sepsis. Other sepsis
Conditions
Interventions
Intervention 1: Control group: Control group: A group of patients admitted to the intensive care unit who will be randomly selected. This group will be candidates for receiving only routine and standa
Sponsors
Rasht University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Clear detection of fluid accumulation of 10%of body weight Electrolyte levels and kidney function should be within normal or acceptable ranges Filling out the informed consent form
Exclusion criteria
Exclusion criteria: Presence of severe underlying diseases Patients with severe acute or chronic illnesses Severe rhythms or drug sensitivity contraindications
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Systemic complications. Timepoint: Daily. Method of measurement: Measurement of body temperature, pulse rate per minute, respiratory rate per minute and blood pressure. | — |
Secondary
| Measure | Time frame |
|---|---|
| Hospital stay. Timepoint: At the beginning of treatment and 48 hours after injection. Method of measurement: It is recorded based on patient records.;Mortality. Timepoint: At the beginning of treatment and 48 hours after injection. Method of measurement: It is recorded based on patient records.;Examination of biochemical indicators. Timepoint: At the beginning of treatment and 48 hours after injection. Method of measurement: It is recorded based on patient records. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr.Anoush Dehnadi Moghadam
Rasht University of Medical Sciences
Outcome results
None listed