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临床试验/NCT00949299
NCT00949299终止4 期

Effects of Buprenorphine on Ulnar Nerve Motor Block

University of Zurich2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2010年1月最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
终止
入组人数
20
试验地点
2
主要终点
The principal aim of the study is to measure the speed of onset and the time of recovery of motor blockage achieved by lidocaine and buprenorphine

研究概览

简要总结

Recent reports showed that the opioid buprenorphine is a very potent sodium channel blocker. Buprenorphine not only exerts a strong antinociception, but also a long lasting antihyperalgesic effect. This antihyperalgesic effect is not observed for other clinically employed opioids but is common for local anaesthetics.

The principal aim of the study is to compare the speed of onset and the time of recovery of motor blockage achieved by lidocaine and buprenorphine, respectively. The investigators hypothesize that the blocking capacity of buprenorphine is equal to the one of lidocaine.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Double (Participant, Investigator)

入排标准

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

入选标准

  • Age: 18 - 65 years
  • Weight: 50-100kg
  • Height: 155-195cm
  • Signed and dated informed consent
  • Sufficient command of German language

排除标准

  • Contraindications to the class of drugs under study
  • Vulnerable subjects (intellectually or mental impaired)
  • Known hypersensitivity to class of drugs or the investigational product
  • Known peripheral neuropathies
  • Diabetes mellitus
  • Chronic alcohol consumption
  • Congestive heart disease
  • Participants of other studies during study period

结局指标

主要结局

The principal aim of the study is to measure the speed of onset and the time of recovery of motor blockage achieved by lidocaine and buprenorphine

时间窗: 6 hours

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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