跳至主要内容
临床试验/NCT05320601
NCT05320601已完成不适用

Efficacy of Peripheral Magnetic Stimulation Compare to Dry Needling in Patient With Upper Trapezius Myofascial Pain Syndrome

Mahidol University1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2022年4月11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
32
试验地点
1
主要终点
Change of Visual analog scale

研究概览

简要总结

Compare efficiency between repetitive peripheral magnetic stimulation and dry needling in patient with upper trapezius myofascial pain syndrome.

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 (Care Provider, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with myofascial pain syndrome at unilateral upper trapezius muscle and had pain score (Visual analog scale) at least 4

排除标准

  • Patients with signs and/or symptoms of neurological deficit
  • Patients with history of cervical hernia, cervical radiculopathy, cervical myelopathy, fibromyalgia, whiplash spondylosis and cervical spinal stenosis.
  • Patients who received physical therapy/injection/surgery at neck or pain area in last 6 months.
  • Patients with abnormal coagulopathy and/or currently use anticoagulant medicine.
  • Patients with cardiac device.
  • Patients with history of aneurysm clip procedure, stent-coils procedure or cochlear implant surgery.
  • Pregnancy

结局指标

主要结局

Change of Visual analog scale

时间窗: Change from baseline Visual analog scale at immediately after intervention, Change from Baseline visual analog scale at 1 week and Change from baseline Visual analog scale at 4 weeks

Pain measurement Score from 0-10, 0 means no pain and 10 means maximum pain. Higher scores mean worse outcome.

次要结局

  • Neck disability index(Change from baseline Neck disability index at immediately after intervention, Change from Baseline Neck disability index at 1 week and Change from baseline Neck disability index at 4 weeks)

研究者

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

Apiphan Iamchaimongkol, MD

Principal Investigator

Mahidol University

研究点 (1)

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