EUCTR2014-004313-82-FI进行中（未招募）不适用
Efficacy and safety of epidural oxycodone
Anaesthesia and Operative Services, Kuopio University Hospital0 个研究点开始时间: 2014年11月25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
- •Women aged 18–75 yr undergoing elective gynaecological surgery with planned postoperative epidural analgesia. Patients must provide written consent.
- •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 100
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 50
排除标准
- •Patient is unwilling to give consent, has allergy/hypersensitivity to oxycodone or other ingredients in the formulations, has reduced respiratory function, has defects in the vertebral column that are likely to hinder the placement of epidural and spinal catheters, is pregnant or nursing, has a tendency for bleeding or is currently on an anticoagulant therapy, or who has used oxycodone during the previous week, or MAO, CYP3A, or CYP2D6 inhibitors during the previous month, cancer surgery.
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