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临床试验/KCT0000183
KCT0000183已完成未知

Efficacy of ramosetron and palonosetron on patient-controlled analgesia related postoperative nausea and vomiting in gynecological laparoscopic surgery -randomised controlled trial

Konkuk University0 个研究点目标入组 320 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
320

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 100(Year)(—)
性别
Female

入选标准

  • Patients undergoing gynaecologic laparoscopic surgery with intravenous PCA for postoperative pain control were enrolled. The patients were American Society of Anesthesiologists Patient Status (ASA PS) I or II, and at least 18 years old.

排除标准

  • Patients were excluded if the following criteria present: 1) urgent or emergent case, 2) re-do case, 3) allergy to egg or soybean oil, 4) history of drug abuse, 5) receiving current medications, 6) concurrent other surgery, 7) surgery within 1 hour and 8) discharge within 72 hours.

研究者

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