跳至主要内容
临床试验/ISRCTN57227250
ISRCTN57227250已完成4 期

Prophylaxis of postoperative nausea and vomiting in cesarean section under spinal anesthesia with intrathecal morphine: controlled clinical trial comparing ondansetron vs placebo vs dexamethasone

Industrial University of Santander (Universidad Industrial de Santander)0 个研究点目标入组 300 人开始时间: 2016年7月17日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
300

研究概览

简要总结

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 1. Pregnant patients scheduled for elective caesarean
  • 2. Age between 18 - 40 years old
  • 3. Spinal (Subarachnoid) anesthesia with intrathecal morphine
  • 4. ASA Physical status 1-2

排除标准

  • 1. Preeclampsia
  • 2. Eclampsia
  • 3. Kidney and/or liver failure
  • 4. Known allergy to ondansetron or dexamethasone
  • 5. Heart disease
  • 6. Vertigo
  • 7. Hyperemesis gravidarum
  • 8. Nausea and vomiting or itching
  • 9. Previous cesarean section
  • 10. 5 HT3 antagonists or corticoids allergy
  • 11. Gestational diabetes
  • 12. Immunosuppression
  • 13. Congenital long QT syndrome
  • 14. Neurological or psychiatric illness that would prevent obtaining consent for the study Emergency Caesarean

研究者

发起方
Industrial University of Santander (Universidad Industrial de Santander)

相似试验