This randomized, double-blind clinical trial was carried out in 120 patients undergoing spine surgery. The study was approved by the Ethics Committee of Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran, with IRCT registration number IRCT2016011225982N1. The inclusion criteria were having an age of 20 to 50 years, ASA class I or II, and spine surgery. The exclusion criteria included patients with hypertension, diabetes, pregnancy, coagulation disorders, ischemic heart disease, history of beta-blockers or calcium channel blockers intake, drug or alcohol abuse, and the operating time of over 150 minutes.
The patients were randomly divided into three groups. Group C received oral clonidine 0.2 mg tablets, 90 minutes before entering the room and 100 cc saline as placebo 15 minutes before anesthesia induction. Group D received placebo pills and 0.5 µ/kg dexmedetomidine 15 minutes before anesthesia induction for 10 minutes in 100 cc saline infusion and 0.25 µ/kg/h continuous infusions during the operation. Group P received placebo tablets and 100 cc saline infusion 15 minutes before anesthesia induction and during the operation as the control group.
All patients were monitored before starting anesthesia with standard monitoring (ECG monitoring, pulse oximetry, and noninvasive blood pressure monitoring). They received 7 cc/kg ringer solution using a peripheral IV line. General anesthesia was induced with midazolam 0.05 mg/kg, fentanyl 3 mcg/kg, sodium thiopental 5 mg/kg, and atracurium0.5 mg/kg. The anesthesia was maintained using 1% isoflurane in the oxygen and N2O mixture. In addition to standard monitoring, a radial arterial line was inserted. Heart rate, systolic, diastolic, and mean arterial pressure were monitored before intubation as the baseline and after intubation, 15, 30, and 60 minutes after starting the surgery, and after extubation.
The amount of intraoperative blood loss was estimated based on the volume of blood in the suction bottle and the number of the blood-soaked gauze pads (20 mL for a completely blood-soaked gauze and 50 mL for a completely blood-soaked long gauze). Recording of the vital signs and the amount of blood loss in each patient was done by an assistant anesthesiologist who was unaware of the study groups.
3.1. Statistical Analysis Methods
The data are reported based as means ± standard deviation. The significance level was set at P < 0.05. In order to compare the obtained data between the groups, the normal distribution of data was studied using the analysis of variance (ANOVA) and chi-square tests. All statistical analyses were performed using SPSS software (version 19).