Neutrophil Lymphocyte ratio.
Conditions
Interventions
Intervention group: In this study, all 90 eligible patients are monitored after general anesthesia and their symptoms are recorded. Also, before and after general anesthesia and when entering recovery
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patients 18 to 60 years old Anesthesia class I and II according to ASA criteria Candidate for surgery under general anesthesia Informed consent to enter the study
Exclusion criteria
Exclusion criteria: Hemodynamic disorders Use of psychotropic or sedative drugsAddiction to opioid and non-opioid drugs BMI (Body Mass Index)>30Cardiovascular diseases Pregnancy and breastfeeding Having diabetes, orthostatic hypotension, bradycardia, hypokalemia, hypothyroidism, depression, long QT syndrome
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Neutrophil to lymphocyte ratio. Timepoint: Before anesthesia, after intubation, 20min after general anesthesia, enterance to the recovery unit. Method of measurement: Venous blood sample. | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood Pressure. Timepoint: Before anesthesia, after intubation, 20min after general anesthesia, enterance to the recovery unit. Method of measurement: Sphygmomanometer. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactPeyman Farhanian
Esfahan University of Medical Sciences
Outcome results
None listed