ACTRN12606000201572尚未招募4 期
The effect of rate of administration of tramadol on the incidence of post operative nausea and vomiting after any surgical operation for which significant postoperative pain is expected
ANZCA (australaian and New Zealand College of Anaesthetists)0 个研究点目标入组 150 人开始时间: 2006年5月29日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 150
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
- 18 Years 至 50 Years（—）
- 性别
- All
入选标准
- •English spoken as first language, or fluent as a second language• Scheduled to have elective non-abdominal surgery under general anaesthesia (including general, orthopaedic, plastic, ENT, urologic, dental or vascular surgery) • Requiring general anaesthesia• Significant post-operative pain requiring opioid therapy expected.
排除标准
- •Inadequate English comprehension• History of allergy or sensitivity to tramadol or morphine• History of previous episode of significant post operative nausea and vomiting• History of significant motion sickness• Epilepsy• Administration of tramadol within previous 36 hours• American Society of Anaesthesiologists’ (ASA) physical status IV or V, reflecting serious cardiorespiratory co-morbidity.• Currently taking selective serotonin receptor inhibitor, tricyclic antidepressant or monoamine oxidase inhibitor drugs• Currently taking prophylactic antiemetics• Pregnancy.
研究者
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