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IRCT20160307026950N56 IRCT 2023-12-25 Esfahan University of Medical Sciences Comparing the effect of laryngoscopy on hemodynamic status and Neutrophil to Lymphocyte Ratio (NLR)after induction of anesthesia Ethomidite, Propofol and Ketamine NLR Comparing the effect of laryngoscopy on hemodynamic status and Neutrophil to Lymphocyte Ratio (NLR)after induction of anesthesia Ethomidite, Propofol and Ketamine 2023-12-06 anticipated 90 Complete https://irct.ir/trial/74113 observational Randomization: N/A, Blinding: Triple blinded, Placebo: Not used, Assignment: Single, Purpose: Diagnostic, Blinding description: This is a three-way blind clinical trial so that before obtaining consent, the patients are included in the study, but the patient does not know which people are included in the study, and it is assumed that the conditions are the same for everyone, the samples are also inside the tube. Identical forms that only have the characteristics and code of the patient group are placed so that the laboratory experts are also kept blind, those responsible for collecting data, and those who evaluate the outcome also do not know about the patient group are blind. 2 Neutrophil Lymphocyte ratio. 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, cbc blood samples are taken from the patient to measure the Neutrophil to Lymphocyte Ratio.. No - There is not a plan to make this available Justification or reason for not sharing IPD is There is no more information
public Peyman Farhanian
Hezar jarib
Isfahan Iran (Islamic Republic of) 8143743561 +98 31 3212 3974 Leylarafiei943@gmail.com Esfahan University of Medical Sciences scientific Behzad Nazem roaya
Hezar jarib
Isfahan Iran (Islamic Republic of) 8146713543 +98 31 3620 2020 behzad_nazem@med.mui.ac.ir Esfahan University of Medical Sciences Iran (Islamic Republic of) 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 18 years 65 years Both 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 Diagnosis 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, cbc blood samples are taken from the patient to measure the Neutrophil to Lymphocyte Ratio. Neutrophil to lymphocyte ratio. Timepoint: Before anesthesia, after intubation, 20min after general anesthesia, enterance to the recovery unit. Method of measurement: Venous blood sample. Blood Pressure. Timepoint: Before anesthesia, after intubation, 20min after general anesthesia, enterance to the recovery unit. Method of measurement: Sphygmomanometer. Esfahan University of Medical Sciences Approved 2023-10-23 Ethics Committee in Biomedical Research, Isfahan University of Medical Sciences Hezar jarib Isfahan Isfehan Iran (Islamic Republic of)