KCT0006113已完成未知
Pragmatic randomized controlled trial of non-pharmacological treatment for lumbar disc herniation : A pilot study
Jaseng Hospital of Korean Medicine0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症
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. Numeric rating scale (NRS) score of radiating pain 5 or more for recent 3 serial days.
- •2. Onset time of radiating pain occurred within 12 weeks.
- •3. Radiologically diagnosed with lumbar disc herniation in lumbar spine magnetic resonance imaging (L-spine MRI)
- •4. 19-70 years old
- •5. participants who agreed and signed informed consent form
排除标准
- •1. Spine metastasis of cancer, acute fracture of spine, or spine dislocation
- •2. Progressive neurologic deficits or severe neurologic deficits
- •3. Soft tissue diseases that can induce low back pain(ie. cancer, fibromyalgia, rheumatoid arthritis, gout,etc)
- •4. Presence of chronic underlying disease which can interfere the efficacy or interpretation (ie. stroke, myocardial infarct, kidney disease, dementia, diabetic neuropathy, epilepsy, etc)
- •5. Concurrent use of steroids, immunosuppressants, orpsychotropic medications or any other medication that can interrupt the study result
- •6. Hemorrhagic disease, severe diabetes or taking anticoagulant drug
- •7. Participants who took NSAIDs or pharmacopuncture within 1 week
- •8. Pregnant or lactating women
- •9. Participants who had undergone lumbar surgery within 3 months
- •10. Participants who had participated in other clinical trial within 1 month, 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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