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临床试验/KCT0003896
KCT0003896招募中未知

A Clinical Trial to Evaluate the Analgesic Efficacy and Safety of Nefopam(Acupan®) Compared to Oxycodone (Oxynorm®) in Postoperative Intravenous Patient-Controlled Analgesia of Patients Undergoing General Surgery

Asan Medical Center0 个研究点目标入组 246 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
入组人数
246

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
20(Year) 至 70(Year)(—)
性别
All

入选标准

  • Patients undergoing general anesthesia under laparoscopic gastrointestinal or colorectal surgery
  • - Patients who applied for postoperative intravenous patient-controlled analgesia
  • - American Society of Anesthesiologists Physical Status 1, 2, and 3

排除标准

  • - Patients taking pain medication preoperatively
  • - Patients who are anaphylactic to nefopam or oxycodone
  • - Patients with estimated glomerular filtration rate <60 ml / min / 1.73 m2
  • - Patients with a history of epilepsy
  • - Patients with a history of ischemic heart disease
  • - Patients taking monoamine oxidase inhibitor
  • - Patients with walking disorders
  • - Patients who can not press the analgesic administration button themselves for pain relief when there is postoperative pain due to impaired cognitive function or comprehension.

研究者

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