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临床试验/IRCT20201028049175N6
IRCT20201028049175N6招募中3 期

Effect of combined Paracetamol(Apotel) and Dexamethasone versus Paracetamol(Apotel) on post operative nausea vomiting after cesarean section

Arak 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 45 years(—)
性别
Female

入选标准

  • Age between 18-45 years
  • Having informed consent
  • Having ASA I and II
  • Nulliparous
  • Singleton pregnancy
  • Patients with elective cesarean
  • Patients with spinal anesthesia
  • Patients with Pfannenstiel incision in surgery.

排除标准

  • Underlying disease (i.e renal, liver, cardiac and pulmonary disease)
  • History of allergy to the drugs of study
  • Addiction or long term using of opiate
  • Coagulopathy or use of anticoagulant drugs
  • Disability for pain scoring
  • Suffering from preeclampsia or HELLP or eclampsia or hepatitis
  • Urgency cesarean section

研究者

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