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临床试验/NCT02429141
NCT02429141已完成不适用

The Ultrasound Guided Periarterial Injection Technique To Axilary Brachial Plexus Block Versus Perineural Multiple InjectionTechnique

North American Institute for Continuing Medical Education (NAICE)1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2015年1月1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
50
试验地点
1
主要终点
Block procedure time for the axillary brachial plexus block

研究概览

简要总结

In the transarterial technique for axillary brachial plexus block, the axillary artery is intentionally punctured to indicate placement of the needle within the neurovascular sheath; local anesthetic is then injected deep and superficial to the axillary artery.

详细描述

To lessen the risk for hematoma and intravascular injection, several modifications, such as the multi-injection perineural technique, have become popular. These techniques require a high degree of technical skill and multiple needle passes, and also carry potential for injury. In this study, the investigators will compare an ultrasound-guided equivalent of the transarterial technique (periarterial injections) to a commonly used multi-injection perineural technique.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Inclusion criteria:
  • Patients (ASA physical status I-III) scheduled to undergo hand or wrist surgery under axillary brachial plexus block

排除标准

  • Patients with pre-existing neuropathy
  • Patients with allergy to local anesthetics
  • Patients with prior surgery in the ipsilateral axilla
  • Pregnant patients
  • Patients with difficulties in communication

结局指标

主要结局

Block procedure time for the axillary brachial plexus block

时间窗: time of the block achievement will be recorded up to 15 minutes

次要结局

  • Onset of the block(outcome measure will be measured up to 30 minutes a)
  • Time to request pain medication(participants will be followed for 3 days)
  • Block success rate(participants success or block failure within 24 hours)

研究者

发起方
North American Institute for Continuing Medical Education (NAICE)
申办方类型
Other
责任方
Principal Investigator
主要研究者

Catherine Vanderpitt, MD

Catherine Vanderpitte, MD

North American Institute for Continuing Medical Education (NAICE)

研究点 (1)

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