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临床试验/NCT02631122
NCT02631122已完成不适用

Ultrasound Guided Supraclavicular Brachial Plexus Block vs Retroclavicular Brachial Plexus Block: Comparison of Impact on Ipsilateral Diaphragmatic Function

Brigham and Women's Hospital2 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2017年12月7日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
44
试验地点
2
主要终点
Incidence of IIpsilateral Diaphragmatic Paresis

研究概览

简要总结

The aim of this study is to evaluate differences between ultrasound guided supraclavicular versus retroclavicular brachial plexus blocks: two similar brachial plexus nerve block techniques that differ in their needle trajectory and injection site.

详细描述

To date, there has not been a study that has compared clinically the retroclavicular brachial plexus block to the supraclavicular brachial plexus block or other brachial plexus blocks. The aim of this study is to evaluate differences between ultrasound guided supraclavicular versus retroclavicular brachial plexus blocks, with primary focus on the incidence of diminished ipsilateral hemidiaphramatic excursion (ipsilateral phrenic nerve blockade). We will also evaluate differences between the two techniques in the success of producing surgical anesthesia, procedural time to perform the block (including imaging time and needling time), block onset time, ease of quality ultrasound needle visualization, and incidence of paresthesias, vascular puncture and pneumothorax. Lastly, we will observe and compare the distribution of motor and sensory blockade of the two techniques

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
Triple (Participant, Investigator, Outcomes Assessor)

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

  • patients scheduled for lower arm surgery
  • patients aged 18 years or older
  • patients ASA class I-III

排除标准

  • Patients unable to cooperate or consent to the study
  • pre-existing neuropathy
  • significant pulmonary disease
  • contralateral phrenic nerve or diaphragmatic dysfunction
  • allergy to local anesthetics
  • infection at needle insertion site
  • history of coagulopathy
  • BMI > 40 kg/m2

结局指标

主要结局

Incidence of IIpsilateral Diaphragmatic Paresis

时间窗: 30 minutes post block, then postoperatively

As evidence by ipsilater diagphragmatic excursion measured by Mmode ultrasound

次要结局

  • Anesthetic and analgesic efficacy(30 minutes post block, then postoperatively)
  • Procedural times (imaging time and needling time), onset time, ease of placement, and block duration(at the time of block)
  • Complication rates(1 day)
  • Nerve block distribution(30 minutes post block)

研究者

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

Kamen Vlassakov

Director of Regional and Orthopedic Anesthesiology

Brigham and Women's Hospital

研究点 (2)

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