跳至主要内容
临床试验/IRCT20110306005993N3
IRCT20110306005993N3已完成3 期

Comparsion of intraincisional bupivacaine, tramadol and bupivacaine plus tramadol in postoperative pain in elective cesarean section patients

Mazandaran University of Medical Sciences0 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
3 期
状态
已完成
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

入排标准

年龄范围
15 years 至 45 years(—)
性别
Female

入选标准

  • Age between 15-45 years
  • Have informed written consent to cooperate with the study
  • Patient classification in class ASA1,2

排除标准

  • The patient refused to continue collaborating in this study
  • Adequate spinal anesthesia and its conversion to general anesthesia
  • Allergy to any of the drugs used
  • History of addiction
  • Existence of underlying pain such as back pain, headache
  • History of using psychiatric drugs
  • Get preoperative housing
  • History of addiction

研究者

相似试验

Comparsion of intraincisional bupivacaine, tramadol... | 临床试验