The agreement of the study was confirmed by the Ethical Committee of Anesthesiology Department, Guilan University of Medical Sciences.
In a double-blind randomized and placebo-controlled clinical trial, 60 patients of those who were admitted for orthopedic surgery during the six months in Poursina hospital, included in this study. P value of 0.05 and a power of 80 % were considered based on the study of Kiran and Evans (
12,
13). After obtaining the informed consent, the patients were assigned randomly in two different groups. Inclusion criteria were adult patients who scheduled for elective lower limb orthopedic surgery, aged between 20-60 years and classified into ASA 1 and 2. The patients who refused to fill out the informed consent or had any history of addiction, cardiac arrhythmia or renal disease were excluded from the study. Besides, if the operation took more than 90 minutes, the patient was excluded from study. Then, the patients were randomly classified into two groups, according to the table of random number. A resident of anesthesiology visited the patients before the operation and described the VAS for them. Meanwhile, he prescribed the premedication and 8 hours NPO for the patients. All of the patients were anesthetized by an anesthesiologist who was blinded to study and didn't participate in data collection. Furthermore, the anesthesiology resident who collected post-operative data were blinded to study and this process continued to end of the study. All the patients were fully informed about the study and blinded to their groups. Spinal anesthesia was done on all patients and each patient received 700 mL of normal saline over 15 min .Then , under sterile situation, 25 g whitacre spinal needle was inserted through L4-L5 intervertebral space, spinal blockade was performed by 100 mg (2 mL) of sterile, Lidocaine 5 % was injected regularly, and an appropriate sensory block level (T6-T7) was checked. Patients were divided in two groups; control and drug group that is S (sufentanil) and S + M (sufentanil + MgSO
4), respectively. A patient - controlled intravenous pump (270 mL) (Chang hi China factory, China) was installed in both groups with an infusion rate of 5 mL /h. In control group, the PCA pump contains 40 mL sufentanil (200 mcg; Janssen-Cilag company, Belgium) plus 230 mL of normal saline whereas in drug group (S + M), the tank contains 40 mL sufentanil with 2000 mg MgSO
4 20 % (Samen Factory, Mashhad) with a total volume of 270 mL. Patients were evaluated at 6, 12, 24, 36 and 48 hours after filling the pump. Need to mention that all patients who transferred to recovery room were administered with PCA pump. So, the magnesium sulfate was infused through the PCA pump over 24 hours at the end of the operation in recovery room, without subsequent infusion. As mention above, the operation usually takes less than 90 min. The patient's primary states were pain score, nausea and vomiting, restfulness; and satisfaction were recorded in questioner. The pain score was estimated based on visual analog scale from zero (pain free) to 10 (maximum level of pain). Nausea and vomiting scored from 1 to 4 (1 = without nausea and vomiting, 2 = nausea without vomiting, 3 = less than two times vomiting, 4 = severe vomiting more than two times) and satisfaction scored from 1 to 4 (1 = low, 2 = intermediate, 3 = good, 4 = excellent) (
14,
15). The restlessness score was estimated based on Ramsay criteria from 1 to 6 scoring system (
16). The patients with pain scores more than 3 were treated with 30 mg of intravenous Mepridine and number of injections were recorded. This dosage of Mepridine could be repeated per 30 minutes and after each pethidine administration, the side effects were monitored. All of these data were registered in questioner paper. The data were analyzed using SPSS 16. The quantitative data such as mean and standard deviation and two qualitative data such as frequency rate and percentage have been shown in all cases, P < 0.05 was considered statistically significant.