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Abstract
This prospective, randomized study was designed to compare two different oral doses of gabapentin(600, and 900 mg) on the total duration of analgesia as a primary outcome, postoperative nausea and vomiting, and level of sedation when administered one hour pre operatively to parturient undergoing elective cesarean section under spinal anesthesia . It also compared the influence of their use on the neonatal outcome. Forty five parturient were randomly allocated into three equal groups. (GC group) for control group, (G600 group) for gabapentin 600mg and (G900 group) for gabaentin900 mg