EUCTR2010-018450-12-SE进行中（未招募）不适用
Optimising pain control after caesarean section - an evaluation if oxycodone can replace morphine and low potency opioids postoperatively. - Cesarean section and pain control
Agneta Blanck Olerup0 个研究点目标入组 80 人开始时间: 2010年6月24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
- 入组人数
- 80
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
- •Women undergoing elective cesarean section at the Karolinska University Hospital.
- •Women who intend to breast feed.
- •Are the trial subjects under 18? yes
- •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
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Women with previous chronic pain, mental illness requiring medication, drug abuse or difficulties to communicate, severe pregnancy complications, premature delivery, medical disease that can be suspected to influence the wellbeing of the newborn baby, intolerance to opiates or other drugs used in the present study or participation in another clinical trial during the last month.
研究者
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