This study is being conducted to investigate the effectiveness and safety of acupuncture for alleviating pain of spondylosis.
This study is being conducted at the Daegu Catholic University Medical Center. Enrolled participants will be randomized into two groups : acupuncture treatment plus epidural block and epidural block alone. This trial will include treatments during 3 weeks, and then follow up after 2 weeks. Participants will have acupuncture treatments of three times per week and epidural block of once per week. All examinations and treatments will be provided free of charge. Compared with epidural block group, acupuncture plus epidural block group will give more effectiveness for alleviate pain caused by lumbar spondylosis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
14
* BL40, BL60, ST36, GB34 : bilaterally, manual acupuncture. * Two points on 1st bladder meridian nearest location of back pain : bilaterally, electrical acupuncture.
Lumbar nerve block will be performed by using the mixture of dexamethasone (5mg) and mepivacaine (10mg).
Daegu Catholic University Medical Center
Daegu, Kyungsangbukdo, South Korea
RECRUITINGVisual analogue scale(VAS)
This outcome will measure changes in the participant's level of low back pain.
Time frame: Change from baseline to 5 weeks
Short form McGill pain questionnaire
Time frame: Chagnes from baseline to 5 weeks
Oswestry Disability Index
Time frame: Changes from baseline to 5 weeks
Present pain intensity(PPI)
Time frame: Changes from baseline to 5 weeks
Pain vision
A device Pain vision Ⓡ PS-2100 calculates a "degree of pain" in cancer patients in addition to VAS
Time frame: Chagnes from baseline to 5 weeks
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