临床试验/IRCT201201308877N1

IRCT201201308877N1已完成2 期

Treatment of postoperative nausea and vomiting after spinal anestheisa for cesarean delivery: a randomized comparison of midazoalm, ondansetron, and a combination

Isfahan University of Medical Sciences0 个研究点目标入组 132 人开始时间: 待定最近更新: 2018年2月22日

适应症

试验速览

阶段: 2 期
状态: 已完成
发起方: Isfahan University of Medical Sciences
入组人数: 132

研究概览入排标准研究者记录与标识符相似试验

研究概览

简要总结

暂无简介。

研究设计

研究类型: Interventional

入排标准

年龄范围: 18 years 至 45 years（—）
性别: Female

入选标准

•patients with ASA I; age between 18 to 45 years old; scheduled for elective cesarean delivery under spinal anesthesia and signing written informed consent to participate in the present study. Exclusion criteria: patients who had smoking habit; obstetric complications or any evidence of fetal compromise; patients who had history of motion sickness; previous postoperative emesis; gastrointestinal disease or administration of antiemetic medication in the previous 24 hours; having allergy to the study drugs and any contraindication for spinal anesthesia.

排除标准

未提供

研究者

发起方

Isfahan University of Medical Sciences

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