跳至主要内容
临床试验/KCT0007703
KCT0007703已完成未知

Comparison of postoperative nausea and vomiting accoring to manual and target controlled infusion of remifentanil in gynecological patients undergoing pelviscopic surgery - Randomized controlled trial

BCWORLD PHARM0 个研究点目标入组 90 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
90

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 69(Year)(—)
性别
Female

入选标准

  • Patients scheduled for elective gynecological surgery using pelviscopy under general anesthesia

排除标准

  • (1) 18 years old or younger, 70 years old or older
  • (2) Pregnant women
  • (3) Allergic to remifentanil or use is contraindicated
  • (4) Administration of antiemetics or steroids within 24 hours before surgery
  • (5) Obesity with a body mass index of 35 kg/m^2 or more
  • (6) ASA classification III or higher

研究者

发起方
BCWORLD PHARM

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