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| Name | Class |
|---|---|
| Kyung Hee University Hospital at Gangdong | OTHER |
| Kyunghee University | OTHER |
| Korea Institute of Oriental Medicine | OTHER_GOV |
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The purpose of this study is to evaluate the efficacy and safety of east-west collaborative treatment using bee venom acupuncture and NSAIDs on pain intensity, functional status and quality of life of patients with chronic cervicalgia
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Bee Venom Acupuncture | Experimental |
| |
| Loxoprofen | Experimental |
| |
| EWCT : Bee Venom Acupucture and Loxoprofen | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Bee Venom Acupuncture | Procedure | Bee Venom 1:20,000 under BVA Increment Protocol - Increment Protocol as
|
| Measure | Description | Time Frame |
|---|---|---|
| Visual Analogue Scale for bothersomeness | Changes from baseline in VAS at 1st, 2nd, 3rd, 4th and 8th week follow-up |
| Measure | Description | Time Frame |
|---|---|---|
| Neck Disability Index | Changes from baseline in NDI at 2nd, 3rd, 4th and 8th week follow-up | |
| Depression scores on Beck's Depression Inventory | Changes from baseline in BDI at 4th and 8th week follow-up |
| Measure | Description | Time Frame |
|---|---|---|
| Skin Roll Test | Changes from baseline in skinfold thickness and pressure algometer scores at 4th and 8th week follow-up |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Byung-Kwan Seo, PhD., KMD | Kyunghee University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Spine Center, Kyung Hee University Hospital at Gangdong | Seoul | 134-727 | South Korea |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 24746224 | Derived | Seo BK, Lee JH, Kim PK, Baek YH, Jo DJ, Lee S. Bee venom acupuncture, NSAIDs or combined treatment for chronic neck pain: study protocol for a randomized, assessor-blind trial. Trials. 2014 Apr 21;15:132. doi: 10.1186/1745-6215-15-132. |
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| ID | Term |
|---|---|
| C040656 | loxoprofen |
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| Loxoprofen | Drug | 60 mg/Tab, pers os 1Tab tid, for 3 weeks |
|
|
| Quality of Life scores on EQ-5D | Changes from baseline in EQ-5D at 2nd, 3rd, 4th and 8th week follow-up |
| Quality of Life scores on SF-36 | Changes from baseline in SF-36 at 4th and 8th week follow-up |
| Visual Analogue Scale for pain intensity | Changes from baseline in VAS at 1st, 2nd, 3rd, 4th and 8th week follow-up |
| Safety profile | Any adverse events must be documented and reported. | At every visit, up to 2 months |
| Credibility test | Changes from baseline in credibility test at 4th week follow-up |