KCT0007057已完成未知
Pragmatic randomized controlled trial of pharmacopuncture therapy for cervical disc herniation: A pilot study
Jaseng Hospital of Korean Medicine0 个研究点目标入组 84 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
- 84
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 69(Year)(—)
- 性别
- All
入选标准
- •1.Symptoms of cervical disc herniation for less than 12 months
- •2.Numeric Rating Scale (NRS) of neck pain is more than 5
- •3.Symptoms of neuromuscular disease in one or both upper limbs (pain, pull, numbness, sensory abnormalities, motor abnormalities)
- •4.Discrimination findings above protusion, which can explain clinical symptoms on Cervical spine MRI or CT
- •5.19-69 years old
- •6.participants who agreed and wrote informed consents
排除标准
- •1.Case of being diagnosed with a specific serious disease that may cause neck pain(Migration of cancer reaching to spine, acute fracture of spine, spine dislocation)
- •2.Progressive neurologic deficits or severe neurologic deficits
- •3.Cause of pain due to soft tissue disease, not the spine(Cancer, fibromyalgia, RA, goat, or etc.)
- •4.Other chronic diseases(stroke, MI, kidney disease, diabetic neuropathy, dimentia, epilepsy, or etc.) that may interfere with the interpretation of therapeutic effects or outcomes
- •5.Participants taking steroid, immunosuppressant, psychotropic medication, or taking other drugs that may affect outcomes
- •6.Inappropriate or unsafe pharmacopuncture therapy; hemorrhagic disease, taking anticoagulant drug, or severe diabetes patients who are likely to be infected
- •7.Participants who took NSAIDs or pharmacopuncture, acupuncture, physical therapy within 1 week
- •8.Pregnant, planning to get pregnant or lactating women
- •9.Participants who had undergone cervical surgery within 3 months
- •10.Participants who had participated in other clinical trial within 1 month, had participated in other study within 6 months from the date of selection, or have plan for participation in other trial during follow up period of this trial
- •11.Participants who can not write informed consent
- •12.Participants who is difficult to participate in the trial according to investigator's decision
研究者
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