Nausea and vomiting. Nausea and vomiting
Conditions
Interventions
Intervention group: In this study, all 80 eligible patients are monitored after spinal surgery and their symptoms are recorded. Also, before and after spinal surgery and when entering recovery, cbc bl
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 spinal anesthesia Informed consent to enter the study
Exclusion criteria
Exclusion criteria: BMI (Body Mass Index)>30 Cardiovascular diseases and hemodynamic disorders Use of psychotropic or sedative drugs Addiction to opioid and non-opioid drugs 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 spinal, 20 minutes after spinal, when entering recovery, immediately after nausea and vomiting and when discharged from recovery. Method of measurement: Venous blood sample. | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood Pressure. Timepoint: Every 10 minutes from the moment of entering the operating room until the moment of discharge from the recovery. Method of measurement: Sphygmomanometer.;Heart Rate. Timepoint: From the moment of entering the operating room until the moment of discharge from the recovery. Method of measurement: Electrocardiogram.;Oxygen saturation. Timepoint: From the moment of entering the operating room until the moment of discharge from the recovery. Method of measurement: Pulse Oximeter. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahmud Falamarz Fuladi
Esfahan University of Medical Sciences
Outcome results
None listed