KCT0007480尚未招募未知
Clinical pilot study on the development of pelvic malposition diagnosis method for chuna treatment for non-acute low back pain
Pusan National University Korean Medicine Hospital0 个研究点目标入组 60 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational Study
入排标准
- 年龄范围
- 19(Year) 至 65(Year)(—)
- 性别
- All
入选标准
- •1. adult lumbosacropelvic patients(aged 19~65) with non-acute low back pain(onset before more than 2 weeks) and Numeric Rating Scale score above 4
- •2. aged above 19 and below 65
- •3. Body Mass Index under 30 (standard according to Obesity Clinical Practice Guideline of Korean Society for the Study of Obesity)
- •4. patient who is capable of ordinary communication
- •5. participant who has signed the clinical trail consent form with voluntary participation decision
排除标准
- •1. patient with underlying disease which could cause low back pain(vertebral metastasis of tumor, acute fracture and dislocation, polio, etc.)
- •2. patient with absolute contraindication of Chuna Manual Therapy(acute cauda equina syndrome, vertebral dislocation, cerebral aneurysm, etc.)
- •3. patient who is considered inappropriate for the clinical trial by researcher(e.g. lumbosacropelvic operation history, knee operation history, innate vertebral disease, nerve root block operation history, etc.)
- •4. operation or medical procedure is scheduled during the treatment period
- •5. patient with chronic disease which could affect the effect of the clinical study : cardiovascular disease, kidney disease, diabetic neuropathy, dementia, epilepsy, etc.
- •6. patient who has received Chuna Manual Therapy within 2 weeks of clinical study registration
- •7. patient who has participated other clinical trials within 1 month
- •8. patient who is incapable of ordinary communication because of dementia or mild cognition disorder, etc.
- •9. pregnant women
- •10. person who has difficulty with signing the clinical trial consent form or is considered incapable of carrying out the normal clinical trial procedure
- •* In the case the number of enrollment of group with/without pelvic deviation is satisfied, patient is considered as meeting the exclusion criteria 10.
研究者
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