EUCTR2006-000047-26-GB进行中（未招募）不适用
A randomized controlled trial of caudal epidural or intravenous fentanyl on the post-operative analgesia requirements after transurethral endoscopic resection of prostate, bladder neck or bladder tumour. - Caudal epidural or iv fentanyl for transureth endoscopic analgesia
eeds Teaching Hospitals NHS Trust0 个研究点目标入组 44 人开始时间: 2006年2月13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
- 44
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
- All
入选标准
- •Male and Female:
- •Aged over 18 years. There is no upper age limit.
- •Scheduled for bladder outlet surgery
- •Written informed 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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •INR > 1.5 on the day of surgery
- •Pregnant or lactating women- a pregnancy test will be carried out if there is any risk of the patient being pregnant.
- •Platelet count <80 on day of surgery
- •Current Clopidogrel treatment
- •On heparin, including high dose enoxaparin (>40mg once daily)
- •Allergy or intolerance to local anaesthetics or fentanyl
- •Current administration of monamine oxidase inhibitors
- •Other contraindications to caudal epidural analgesia such as local sepsis
研究者
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