KCT0001939
Recruiting
未知
An Integrative Medical Approach of Electroacupuncture with Usual care for Patients with Pain after Back surgery : A Multicenter, Randomized Controlled Clinical Trial, Qualitative and Cost-Effectiveness Research
ConditionsNot Applicable
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not Applicable
- Sponsor
- Korea Institute of Oriental Medicine
- Enrollment
- 108
- Status
- Recruiting
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patients who are between 19 and 70 years of age
- •2\. Patients whose low back pain persisted or recurred after back surgery with or without leg pain and patients whose pain has persisted for at least three weeks recently
- •3\. Patients with pain, defined as a Visual Analogue Scale (VAS) value \= 50mm
- •4\. Patients who agreed to participate voluntarily in this study and signed a written informed consent forms
Exclusion Criteria
- •1\. Patients who have been diagnosed with a serious disease that can cause low back pain (e.g., cancer, spinal infection, inflammatory spondylitis)
- •2\. Patients with a progressive neurological deficit or with severe neurological symptoms
- •3\. Patients whose pain causes are not resulted from spine or resulted from soft tissue diseases (e.g., cancer, fibromyalgia, rheumatoid arthritis, gout)
- •4\. Patients with a chronic disease that could influence the treatment effects or the analysis of the treatment results (e.g., severe cardiovascular disease, diabetic neuropathy, dementia, epilepsy)
- •5\. Patients for whom acupuncture would be inappropriate or unsafe (e.g., hemorrhagic disease, a history of having received anticoagulant therapy, severe diabetes with a risk of infection, severe cardiovascular disease)
- •6\. Patients who are currently pregnant or planning to become pregnant
- •7\. Patients with psychiatric diseases
- •8\. Patients who are participating in another clinical trial
- •9\. Patients who are unable to sign a written informed consent form
- •10\. Patients who are judged by the researchers to be inappropriate for the clinical study
Outcomes
Primary Outcomes
Not specified
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