KCT0007057
Completed
未知
Pragmatic randomized controlled trial of pharmacopuncture therapy for cervical disc herniation: A pilot study
Jaseng Hospital of Korean Medicine0 sites84 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Jaseng Hospital of Korean Medicine
- Enrollment
- 84
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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
Outcomes
Primary Outcomes
Not specified
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