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临床试验/NCT02323282
NCT02323282Unknown4 期

The Study of Ropivacaine Median Effective Concentration in Ultrasound-guided Supraclavicular Brachial Plexus Block

Yu Shan1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2014年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
60
试验地点
1
主要终点
the affection of nerve block

研究概览

简要总结

To determine the median effective concentration of ropivacaine hydrochloride for ultrasound-guided supraclavicular brachial plexus block. The result can provide reference for choosing appropriate drug concentration in clinical anesthesia.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • ASA I or II

排除标准

  • upper limb paresthesia
  • allergic to local anesthetics
  • surgery history of clavicle
  • BMI>30kg/m^2

研究组 & 干预措施

ropivacine

Other

干预措施: ropivacaine (Drug)

结局指标

主要结局

the affection of nerve block

时间窗: 30 minutes

The anesthetic efficacy of five nerves, respectively named lateral antebrachial cutaneous nerve, medial cutaneous nerve of the forearm, radial nerve, median nerve, and ulnar nerve was assessed within 30 min after anesthesia. The next concentration of ropivacaine was adjusted according to the response of the previous patient using up-down sequential allocation.

次要结局

未报告次要终点

研究者

发起方
Yu Shan
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Yu Shan

The study of ropivacaine median effective concentration in ultrasound-guided supraclavicular brachial plexus block

Shanghai Jiao Tong University Affiliated Sixth People's Hospital

研究点 (1)

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