EUCTR2014-003116-37-NO进行中（未招募）不适用
Postoperative analgesia with oxycodone after caesarean section - The oxycodone study
Akershus University Hospital0 个研究点开始时间: 2015年5月18日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •Healthy women (ASA class 2) between 18 and 45 years with a single fetus undergoing an elective caesarean section under regional anesthesia. They must be at term (between 37+0 and 41+6 weeks pregnant), pre conception BMI (body mass index) between 18.5 and 24.9, height between 155 cm and 180 cm. They must have read and signed the written information.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 50
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Known sensitivity against oxycodone. Women with pre conceptual other diseases (i.e ASA 3 or more)
研究者
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