KCT0007480
Not yet recruiting
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 sites60 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Pusan National University Korean Medicine Hospital
- Enrollment
- 60
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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
Outcomes
Primary Outcomes
Not specified
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