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临床试验/ACTRN12618000429257
ACTRN12618000429257终止4 期

A multicentre, randomised, non-inferiority trial of chewing gum versus ondansetron to treat postoperative nausea and vomiting in female patients after breast or laparoscopic surgery (The Chewy Trial)

Melbourne Health0 个研究点目标入组 212 人开始时间: 2018年3月26日最近更新:
适应症

试验速览

阶段
4 期
状态
终止
入组人数
212

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
12 Years 至 o limit(—)
性别
Female

入选标准

  • Female patients aged 12 years or older, weight 30 kg or more, preoperative Apfel score 2-4, presenting for breast or laparoscopic surgery under volatile-based, general anaesthesia.

排除标准

  • Patients having propofol-maintained general anaesthesia or inhalational induction without propofol co-induction, a contraindication to chewing gum, or any protocolised anti-emetic drug (prophylaxis, intervention or rescue), treatment with any of the study anti-emetic medications within 8 hours of induction of anaesthesia or planned post operative ventilation.

研究者

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