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临床试验/TCTR20200114003
TCTR20200114003已完成4 期

Efficacy of perineural dexamethasone with lidocaine and bupivacaine mixture in axillary brachial plexus block for decreasing duration of motor blockage in patient undergoing surgery for fracture distal end radius: A randomized controlled trial

Faculty of Medicine Siriraj Hospital, Mahidol University0 个研究点目标入组 70 人开始时间: 2020年1月14日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
70

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

年龄范围
20 Years 至 85 Years(—)
性别
All

入选标准

  • 1. Age 20-85 years old
  • 2. Known diagnosed as closed fracture distal end of radius
  • 3. ASA physical status I-III as American Society of Anesthesiologists classification
  • 4. Indication for axillary brachial plexus block for perioperative analgesia for surgery < 3 hours

排除标准

  • 1. Refusal
  • 2. Cognitive impairment
  • 3. Contraindication for axillary brachial plexus block
  • 4. Anatomy deformity in blocking area
  • 5. Neuropathy or neurological deficit
  • 6. DM with HbA1C > 7.5 %
  • 7. GFR < 50 ml/min
  • 8. Body weight below 35 kg
  • 9. Known allergy to intervention agents
  • 10. Chronic pain (take oral morphine > 20 mg/day)

研究者

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