ISRCTN13424423已完成不适用
A double blind, randomised controlled trial to assess the efficacy of bilateral paravertebral blockade for analgesia after cardiac surgery
Imperial College Healthcare0 个研究点目标入组 50 人开始时间: 2015年7月26日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 50
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
- Female
入选标准
- •1. Age 40-70 years
- •2. Undergoing elective and urgent first time coronary bypass surgery
排除标准
- •1. Critical preoperative state
- •2. Single graft surgery (no leg incision)
- •3. Minimally invasive surgery (no sternotomy)
- •4. Significant renal disease (baseline creatinine >150 micromolar: morphine contraindicated)
- •5. Patients exceeding 110kg (4% of our operative population practical difficulties of positioning unconscious patients to place the block)
- •6. Pregnancy
- •7. Patients with chronic pain taking regular analgesic medication
- •8. Patients with a significant abnormality of coagulation
- •9. Participation in another interventional study
- •10. Patients unable to give informed consent
- •11. Hypersensitivity to lidocaine
研究者
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