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临床试验/KCT0007480
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

发起方
Pusan National University Korean Medicine Hospital

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