跳至主要内容
临床试验/IRCT2017062133566N1
IRCT2017062133566N1已完成3 期

The Comparison of the effect of Ondansetron and Apotel on postoperative pain control in patients with upper limb fracture undergoing general anesthesia

Vice chancellor for research, Golestan University of Medical Sciences0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
50

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
15 years 至 90 years(—)
性别
All

入选标准

  • ASA Class 1; Upper limb fracture; Patients who undergo anesthesia with propofol as an anesthetic inducer; Satisfied to participate in the study; being at the age of 15 and older. Exclusion criteria: ASA grade 3 and 4; uncontrolled diabetes; history of ischemic heart disease (IHD); history of stroke; malignancy; psychiatric problems; Pregnancy; surgery duration greater than 120 minutes; history of substance abuse or drug abuse; Alcohol consumption; history of liver problems; history of Apotel (acetaminophen) sensitivity; history of nausea and vomiting after previous surgical procedure; Patients with long Q-T intervals.

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research, Golestan University of Medical Sciences

相似试验