Comparison of changes in Neutrophil-to-Lymphocyte Ratio (NLR) in patients with nausea vomiting and patients without nausea vomiting
Phase 2
Recruiting
- Conditions
- ausea and vomiting.Nausea and vomiting
- Registration Number
- IRCT20160307026950N42
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
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
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
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method eutrophil 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 Outcome Measures
Name Time Method 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.