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临床试验/ISRCTN13419503
ISRCTN13419503已完成不适用

Comparison of two solutions of 1.5% mepivacaine with different sodium concentrations for ultrasound guided popliteal block. A randomised controlled trial

a Paz University Hospital0 个研究点目标入组 66 人开始时间: 2015年9月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
66

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 scheduled for unilateral hallux valgus surgery repair by osteotomy of the first metatarsal type chevron, and intended to be operated by the same surgical team
  • 2. Age between 18 and 80 years
  • 3. Physical status ASA I-III
  • 4. Body mass index (BMI) less than 35 kg / m2

排除标准

  • 1. Existence of any regional anaesthesia contraindication
  • 2. Inability to distinguish the popliteal nerve with ultrasound
  • 3. Cognitive impairment
  • 4. Chronic use of opioids and/or neuroleptic drugs
  • 5. Pregnancy
  • 6. Peripheral neuropathy
  • 7. Patients less than 18 years old or more than 80
  • 8. ASA IV classification
  • 9. Allergy to drugs used in the study
  • 10. Body mass index (BMI) = 35 kg/m2.

研究者

发起方
a Paz University Hospital

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