ACTRN12609000006246已完成4 期
An evaluation of the safety and effectiveness of patient-controlled intranasal fentanyl for relieving pain in birthing women.
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 50
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
- 18 Years 至 o limit（—）
- 性别
- Female
入选标准
- •18 years old and over;
- •Singleton pregnancy;
- •Term – at least 37 weeks;
- •Prima Gravida.
排除标准
- •Failure to provide consent;
- •Complicated pregnancy – i.e. – no pregnancy induced hypertension, pre-eclampsia, gestational diabetes mellitus;
- •Abnormal foetal positioning i.e. breech;
- •Placental abnormalities;
- •Non-singleton pregnancy;
- •Allergy to opioid analgesia;
- •Bronchial asthma
- •Myasthenia gravis;
- •Opioid Tolerance including regular use of methadone, buprenorphine, heroin, morphine, oxycodone;
- •Chronic nasal problems i.e. hay-fever, sinusitis, common cold;
- •Inability to self administer Patient-Controlled Intranasal Fentanyl (PCIF).
研究者
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