ACTRN12619001345178已完成未知
Patient controlled oral analgesia (PCOA) for women following caesarean section delivery: A Non inferiority study.
Johanna Pigou0 个研究点目标入组 38 人开始时间: 2019年10月1日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 38
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
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 16 Years 至 o limit（—）
- 性别
- Female
入选标准
- •Women having a caesarean section at Hutt Hospital.
排除标准
- •Catagory 1 emergency caesarean section
- •Any emergency caesarean section in which the woman in not in a position to give consent including due to time pressure, pain, feeling overwhelmed
- •Allergy or significant adverse reaction to paracetamol, ibuprofen or tramadol
- •Pre-eclampsia and HELLP syndrome
- •Seizure disorder requiring anti-epileptics
- •Documented history of drug misuse of mother or partner
- •Inability to understand PCOA process for example due to Intellectual/cognitive impairment, Language barriers
- •Risk of serotonin syndrome
- •The woman does not wish to participate
研究者
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