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临床试验/IRCT20110712007013N27
IRCT20110712007013N27招募中3 期

Comparing the effect of Dexmedetomidine-Paracetamol combination and placebo in prevention of postoperative pain in patients undergoing cesarean delivery with spinal anesthesia

Tabriz University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
100

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
18 years 至 40 years(—)
性别
Female

入选标准

  • Pregnant women between the ages of 18 and 60 years old
  • ASA class one and two
  • Candidates for elective cesarean section or spinal anesthesia

排除标准

  • Sensitivity to the compounds used for intervention group
  • Mental illness
  • Patients with cardiovascular, pulmonary, liver and kidney and ...disease
  • Multiple pregnancy
  • Urgent cesarean

研究者

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