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Study aim
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Comparison of low-dose intravenous of Propofol and Lidocaine on the reduction of local pain caused by intravenous injection of full-dose Propofol during anesthesia induction.
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Design
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This randomized, double-blind, parallel-group, phase 2-3 clinical trial will be conducted on 88 patients 18 to 60 years who are candidates for elective surgery under general anesthesia using a block randomization.
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Settings and conduct
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In operating room, after fixing a 20G angiocatheter in the veins on the back of the patient's hand, the hand is held up for 10 seconds and a tourniquet is tied at the top of the angiocatheter and one of two drugs, propofol and lidocaine, is injected in syringes of the same volume and shape. After 2 minutes, the vein is opened and 0.5 mg/kg propofol is injected and the intensity of hand 's pain is recorded based on the VAS. Then the rest of the propofol (1.5 mg/kg) is injected along with the other induction drugs, and the patient is then intubated.
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Participants/Inclusion and exclusion criteria
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Inclusion:18-60 years; ASA class1&2; Elective surgery under general anesthesia.Exclusion: Cardiovascular disease; Seizures;Use of narcotics and sedatives; Food and drug allergies; Infection or wounds on the back of the hands.
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Intervention groups
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In operating room, after fixing a 20G angiocatheter in the veins on the back of the patient's hand, the hand is held up for 10 seconds and a tourniquet is tied at the top of the angiocatheter. Then, one of the two drugs, lidocaine (40 mg) or propofol (20 mg), is injected. After 2 minutes, the vein is opened and 0.5 mg/kg propofol is injected. Then, the intensity of pain in the patient's hand during the injection of propofol is recorded based on the VAS. Finally, anesthesia is induced by injecting the rest of the propofol (1.5 mg/kg) and the other drugs, and intubation will be performed after 3 minutes.
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Main outcome variables
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Intensity of hand pain