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临床试验/TCTR20210611005
TCTR20210611005已完成4 期

Palonosetron versus ondansetron in preventing intrathecal morphine-induced postoperative nausea, vomiting, and pruritus in cesarean delivery: a double-blinded, randomized, placebo-controlled trial

King Chulalongkorn Memorial Hospital0 个研究点目标入组 300 人开始时间: 2021年6月11日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
300

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 N/A (No limit)(—)
性别
Female

入选标准

  • ASAII parturient aged 18 years or above scheduled for elective cesarean delivery under spinal anesthesia

排除标准

  • 1. Known allergy or contraindication to ondansetron, palonosetron, and other drugs in the study protocol
  • 2. Having contraindication to or refusal of spinal anesthesia
  • 3. Parturient with pregnancy-related complication such as fetal distress, severe pre-eclampsia
  • 4. Parturient with preoperative symptoms of nausea and vomiting
  • 5. Having coexisting skin disorder or pruritic skin disease
  • 6. A patient who had received antiemetic, emetogenic, or steroid medication
  • 7. The participant who needs an anesthetic technique conversion to general anesthesia

研究者

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