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临床试验/KCT0007421
KCT0007421已完成未知

Thread embedding acupuncture for temporomandibular disorder: Protocol for a pilot randomized controlled trial

Kyung Hee University Oriental Medicine Hospital at Gangdong0 个研究点目标入组 30 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 70(Year)(—)
性别
All

入选标准

  • 1) regional pain in the unilateral or bilateral TMJ and masticatory muscles lasting >3 months intermittently or persistently
  • 2) average pain intensity >40 mm on a 100 mm visual analogue scale (VAS) in the last week. (If the pain is on both sides, the one with the more pain
  • 3) local pain in the jaw, temple, inner ear, or front of the ear caused by jaw movement, function, or parafunction according to the diagnostic criteria for temporomandibular disorders (DC/TMD)
  • 4) myalgia, myofascial pain, or arthralgia identified by palpation assessment of the examiner according to the DC/TMD
  • 5) adults aged 19–70 years who agree to participate in the clinical trial and provide written informed consent.

排除标准

  • 1) Pain caused or aggravated by traffic accidents or traumatic injuries.
  • 2) History of surgery in the temporomandibular joint.
  • 3) History of multiple pain disorders (e.g., rheumatoid arthritis, etc.) or neurological diseases (e.g., brain tumor, stroke, trigeminal neuralgia, etc.) that may interfere with the treatment effects or interpretation of results.
  • 4) Taking steroids, immunosuppressants, psychiatric drugs, or other medication that may affect results.
  • 5) Change in drug-taking history of analgesics, including non-steroidal anti-inflammatory drugs, within a month.
  • 6) History of thread embedding acupuncture (TEA) on the facial region within a month.
  • 7) History of hypersensitivity on TEA or severe keloid scar.
  • 8) Inability to conduct TEA due to skin diseases (inflammation, scar, seborrheic dermatitis, or psoriasis on the treatment location) or blood coagulation disorders.
  • 9) Pregnant women, women who are planning to get pregnant or in the case of lactation.
  • 10) Participation in another clinical trial within a month before the date of selection, or plan to participate in another clinical trial during the treatment and follow-up period
  • 11) Other conditions judged by the researchers to be ineligible to participate in the clinical trial.

研究者

发起方
Kyung Hee University Oriental Medicine Hospital at Gangdong

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