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临床试验/NCT05723354
NCT05723354招募中不适用

Comparison of Clinical Efficacy of Axillary Block in Patients of Cervical Radiculopathy

Keimyung University Dongsan Medical Center2 个研究点 分布在 2 个国家目标入组 70 人开始时间: 2023年2月13日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
70
试验地点
2
主要终点
Numerical rating scale changes among 4 time periods

研究概览

简要总结

The primary endpoint of this study was to compare the clinical efficacy of axillary block in patients of cervical radiculopathy using 2 volumes of local anesthetics.

详细描述

The interscalene brachial plexus block is an effective intervention for reducing postoperative pain but is related to side effects, Suprascapular nerve block and a block of the axillary nerve have been introduced as alternatives to the interscalene brachial plexus for the control of postoperative pain. Previous study demonstrated new method of axillary block using interfascial plane injection guided by ultrasoud. Axillary block has been used widely for the relief of postoperative arm pain.

Recent study deomonstrated good pain relief when ultrasound guided interfascial plane injection was performed in patients with cervical radiuculopathy.

There is no study showing clinical efficacy of interfascial plane injection of axillary block in patients of cervical radiculopathy.

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
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Cervical foraminal stenosis
  • Cervical central stenosis
  • Cervical disc herniation
  • Cervical spondylolisthesis
  • Prominent arm pain rather than neck pain

排除标准

  • Infection
  • Pregnancy
  • allergy to local anesthetic agents
  • previous cervical spine surgery
  • Prominent neck pain rather than arm pain

结局指标

主要结局

Numerical rating scale changes among 4 time periods

时间窗: baseline, 2 weeks after injection, 4 weeks after injection, 8 weeks after injection

Numerical rating scale changes among 4 time periods

Neck disability injex changes between 2 time periods

时间窗: baseline, 8 weeks after injection

Neck disability injex changes between 2 time periods

次要结局

未报告次要终点

研究者

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

Ji Hee Hong

Professor

Keimyung University Dongsan Medical Center

研究点 (2)

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