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临床试验/NCT01636869
NCT01636869已完成4 期

Plasma Concentrations of Bupivacaine After Spinal Anesthesia With Single Shot Femoral Nerve Block and Peri-articular Injection in Total Knee Arthroplasty

Mahidol University1 个研究点 分布在 1 个国家目标入组 43 人开始时间: 2012年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
43
试验地点
1
主要终点
plasma concentration of bupivacaine after spinal anesthesia with single-shot femoral nerve block and periarticular block

研究概览

简要总结

Patients with knee arthroplasty usually performed under spinal anesthesia with a single-shot femoral nerve block and periarticular block, so we would like to know the plasma concentration of bupivacaine in these patients.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
30 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age of 30-70 yr
  • patient undergo total knee arthroplasty under spinal block and single shot femoral nerve block and periarticular block

排除标准

  • patient's refusal
  • allergic to bupivacaine
  • body weight less than 50 kg
  • liver disease
  • heart disease
  • coagulopathy
  • infection at both groin

研究组 & 干预措施

bupicavaine

Experimental

干预措施: Bupivacaine (Drug)

结局指标

主要结局

plasma concentration of bupivacaine after spinal anesthesia with single-shot femoral nerve block and periarticular block

时间窗: 2 hours

次要结局

  • bupivacaine toxicity(24 hr)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Saowaphak Lapmahapaisan

instructor

Mahidol University

研究点 (1)

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