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临床试验/NCT01221415
NCT01221415撤回不适用

A Comparison of Ultrasound and Nerve Stimulator Techniques for Nerve Localization in Regional Anesthesia

Ochsner Health System1 个研究点 分布在 1 个国家开始时间: 2008年1月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
time from injection of local anesthetic to adequate surgical anesthesia

研究概览

简要总结

The primary objective of this study is to compare ultrasound versus nerve stimulator techniques for nerve localization when performing peripheral nerve blocks. Specifically the investigators will be performing Popliteal, Femoral, and Interscalene nerve blocks. The investigators will be looking for differences in 1) time taken to locate the target nerve and inject local anesthetic 2) time from injection of local anesthetic to adequate surgical anesthesia 3) effectiveness of block 4) incidence of vascular puncture 5) incidence of adverse events 6) patient satisfaction.

详细描述

After obtaining informed consent, subjects will be randomized to either the ultrasound or nerve stimulator groups as the method for nerve localization prior to peripheral block placement.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

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

入选标准

  • American Society of Anesthesiologists (ASA) Physical status I-III
  • Arthroscopic knee surgery or Lower leg/foot surgery as well as shoulder arthroscopy
  • Outpatient status
  • Patient preference for a regional anesthetic
  • Subjects should be capable of giving informed consent

排除标准

  • Allergy to:
  • Local anesthetics
  • Hydromorphone
  • Midazolam
  • Patient refusal
  • Infection at the injection site
  • Peripheral Neuropathy

结局指标

主要结局

time from injection of local anesthetic to adequate surgical anesthesia

时间窗: within the first 45 minutes after injection of local anesthestic

次要结局

  • time taken to locate the target nerve and inject local anesthetic(within 45 minutes prior to injection)
  • effectiveness of block(within 1 hour of injection)
  • incidence of vascular puncture(within 30 minutes of injection)
  • incidence of adverse events(within 2 weeks of the day of surgery)
  • patient satisfaction(within 2 weeks of the date of surgery)

研究者

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

Leslie Thomas

Anesthesiologist

Ochsner Health System

研究点 (1)

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