Lumbar Spinal Fusion Surgery. Fusion of spine, lumbar region
Conditions
Interventions
Intervention 1: Control group: After preparing patents for intravenous injection and administration of 500 cc of normal saline before induction of anesthesia, all patients will be pre-oxygenated with
The first group, as a control group, will receive only normal saline intravenously within 10 minutes. Intervention 2: Intervention group: Patients in this group, in addition to induction of anesthesia
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
20 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients who are candidates for lumbar spinal fusion surgery Aged between 20 and 60 years ASA I and II based on America Society of Anesthesiologists (ASA) classification Being consent to participate in the study
Exclusion criteria
Exclusion criteria: Allergy to magnesium sulfate Liver, kidney, cardiovascular failure Opioid use Consumption of NSAIDs Consumption of calcium channel blockers
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Systolic blood pressure. Timepoint: Before surgery, immediately after surgery and 15, 30, 45, and 60 minutes during surgery and in recovery. Method of measurement: Monitoring device.;Diastolic blood pressure. Timepoint: Before surgery, immediately after surgery and 15, 30, 45 and 60 minutes during surgery and in recovery. Method of measurement: Monitoring device.;Hear rate. Timepoint: Before surgery, immediately after surgery and 15, 30, 45 and 60 minutes during surgery and in recovery. Method of measurement: Monitoring device.;Amount of bleeding. Timepoint: During surgery and in recovery. Method of measurement: Blood in suction and gauze. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZahra Rahimi
Esfahan University of Medical Sciences
Outcome results
None listed