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临床试验/TCTR20230713013
TCTR20230713013尚未招募4 期

Comparison of relieving post-needling soreness with repetitive peripheral magnetic stimulation (rPMS) compared with sham

Panyananthaphikkhu Chonprathan Medical Center Srinakharinwirot University0 个研究点目标入组 40 人开始时间: 2023年7月13日最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 60 Years(—)
性别
All

入选标准

  • 1. Patients with myofascial pain syndrome of the upper trapezius muscle with at least one myofascial pain trigger point treated by Deep Dry Needling Muscle and twitching were recorded using ultrasound and recorded in the form of a video clip.
  • 2. Body mass index 19 to 25 kg/m2.

排除标准

  • 1. Patients with metal magnets within the head or treatment area within 30 cm, such as sutures, clips, coils, magnetic dental implants or implanted insulin pumps.
  • 2. Patients with digital therapeutic tools such as pacemakers, implantable cardioverter-defibrillators, vagus nerve stimulators [VNS] and wearable cardioverter-defibrillators.
  • 3. Patients with a history of seizures or uncontrolled seizures.
  • 4. Pregnant women
  • 5. patients with severe or recent heart disease
  • 6. History of treatment with repetitive peripheral magnetic stimulation (rPMS)
  • 7. Have a history of taking painkillers anti-inflammatory drugs and muscle relaxants within 24 hours
  • 8. Have a bleeding disorder such as haemophilia or take blood-thinning medication. (anticoagulant)
  • 9. Has a fear of needles
  • 10. Abnormal skin conditions at the acupuncture site, such as rashes, dermatitis, or infection
  • 11. Allergies to disinfectants used to clean the skin, such as alcohol or povidone-iodine.
  • 12. Allergic to needles or metal
  • 13. Allergic to adhesive plaster or Tegaderm

研究者

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