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The hypothesis of this study is that the improvement of Numeric Rating Scale (NRS) for Pain at the end of the study will be greater in the Wet Cupping Treatment group than in the Waiting Control group.
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Inclusion criteria
Exclusion criteria
Patients who have low back pain due to specific and known etiological causes (infection, tumor, osteoporosis, ankylosing spondylitis, fracture, inflammatory process, radicular syndrome, cauda equinal syndrome).
Patients who are inappropriate to the wet cupping treatment.
Patients who have experiences of wet cupping treatment during last 3 months.
Patients who have had treatment for low back pain during last 2 weeks.
Patients who are in pregnancy or have plan to conception.
Patients who have vertebra surgery or have plan of surgery.
Patients who are inappropriate to join this trial judged by the radiologists or specialists.
Primary purpose
Allocation
Interventional model
Masking
37 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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