Lumbar and Cervical Pain Clinical Trial
Official title:
The Evaluation of the Effectiveness of CAM Treatments for Lumbar and Cervical Spine Pain Patients Due to Spinal Disease : Prospective, Observational Study
NCT number | NCT01791933 |
Other study ID # | JS-CT-2013-01 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | February 2013 |
Est. completion date | October 2013 |
Verified date | November 2018 |
Source | Jaseng Hospital of Korean Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of this study is to investigate the effect of CAM treatments consisting of herbal medicine, Chuna manual therapy, pharmacoacupuncture, acupuncture on lumbar and cervical spine pain patients due to spinal disease.
Status | Completed |
Enrollment | 111 |
Est. completion date | October 2013 |
Est. primary completion date | September 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Patients suffering from low back pain or Neck due to spinal disease Agree to the treatment of more than 2 months - Age all(If under 18yr, Guardian's consent need) - Volunteers do not have a problem with my speech as those who have signed the consent Exclusion Criteria: - Diagnosis of serious disease(s) which are possible causes of back pain such as malignancy, vertebral fracture, spinal infection, inflammatory spondylitis, cauda equina compression, etc. - Prior diagnosis of other chronic disease(s) which could affect effectiveness or interpretation of treatment results such as cardiovascular disease, diabetic neuropathy, fibromyalgia, rheumatoid arthritis, Alzheimer's disease, epilepsy, etc. - Progressive neurologic deficit(s) or concurrent severe neurological symptoms Unsuitable for or at risk of complications from acupuncture treatment such as patients with clotting disorders, severe diabetes with risk of infection, serious cardiovascular disease, or undergoing anticoagulant treatment, etc. - Under prescription of corticosteroids, immuno-suppressant drugs, psychiatric medicine, or other medication considered unsuitable for subjects by the researcher - Experience of gastroenteric complications after taking NSAIDs or currently undergoing treatment for digestive disorders - During pregnancy or suspected pregnancy - Subjects considered unsuitable for clinical trial by the researcher |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Jaseng Hospital of Oriental Medicine | Seoul | Gangnam-gu |
Lead Sponsor | Collaborator |
---|---|
Jaseng Hospital of Korean Medicine |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | NRS of low back pain or neck pain/NRS of radiating pain | Change from Baseline at 3rd month | ||
Secondary | ODI (Oswestry Disability Index) | Baseline, 1st month, 2nd month, 3rd month | ||
Secondary | Patient satisfaction | Patient satisfaction of treatment | 3rd month | |
Secondary | Job loss | Life activity of loss rate | Baseline, 1st month, 2nd month, 3rd month | |
Secondary | painkiller intaken of times | Baseline, 3rd month | ||
Secondary | Adverse reactions | Baseline, 1st month, 2nd month, 3rd month |