ISRCTN37852146进行中（未招募）3 期
Pain Relief After Instrumented Spinal surgEry trial
适应症
试验速览
- 阶段
- 3 期
- 状态
- 进行中（未招募）
- 入组人数
- 456
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. People aged 16 years or over
- •2. Scheduled for elective, posterior lumbar-instrumented spinal surgery +/- decompression
- •3. Able to give informed consent, with interpreters provided where necessary
排除标准
- •1. Patients with drug sensitivity or allergy to any of the trial agents i.e. intrathecal opioid or local anaesthetic
- •2. Patients undergoing fusion at more than three vertebral levels
- •3. Patients with an infection or tumour at the block site or surgical site
- •4. Patients meeting criteria for American Society of Anaesthesiologists Physical Status Classification Grade 4-5
- •5. Patients undergoing surgery during an emergency admission (this would preclude a detailed risk-benefit conversation with a consultant anaesthetist, which our PPI group told us was vital pre-consent).
- •6. Patients scheduled for single-level microdiscectomy and decompression.
- •7. Current pregnancy
研究者
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