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临床试验/ISRCTN31685121
ISRCTN31685121已完成未知

Analgesic efficiency of intrathecal bupivacaine with morphine and bupivacaine alone in lower limb orthopaedic surgery. A comparative study

Platinum Orthopaedic and Spine Clinic0 个研究点目标入组 60 人开始时间: 2022年5月12日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
60

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. Patients undergoing elective lower limb orthopaedic surgery
  • 2. ASA status class I and II
  • 3. Patients between 16 - 60 years of age
  • 4. Patients who were on admission for 72 hours or more postoperatively

排除标准

  • 1. Pregnant or breastfeeding mothers
  • 2. Patients with polytrauma
  • 3. Glasgow coma scale <15
  • 4. Opioids abusers
  • 5. Expected post-surgical stay <24 hours
  • 6. ASA physical status class III and IV
  • 7. Patients allergic to bupivacaine and/morphine
  • 8. Contraindication to spinal anaesthesia

研究者

发起方
Platinum Orthopaedic and Spine Clinic

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