Spinal Cord Injury Clinical Trial
Official title:
The Effect of Botulinum Toxin A in Post Spinal Cord Injury Neuropathic Pain
The purpose of this study is to determine whether botulinum toxin A is effective in the treatment of neuropathic pain in spinal cord injury patients.
Status | Completed |
Enrollment | 40 |
Est. completion date | April 2013 |
Est. primary completion date | April 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 20 Years and older |
Eligibility |
Inclusion Criteria: - more than twenty years of age - paraplegic or tetraplegic due to cervical and thoracic spinal cord injury - more than 12 months since spinal cord injury and ASIA impairment scale unchanged for more than 6 months - persistence of neuropathic pain for more than three months or remission and recurrence of neuropathic pain for more than six months - a pain score of 40mm or more on the visual analogue scale Exclusion Criteria: - neuropathic pain caused by confounding factors other than spinal cord injury - contraindicated for botulinum toxin type A - a change in pain medication one month prior to study enrollment - a condition involving neuromuscular junction (Ex. Eaton Lambert disease, myasthenia gravis) - person who received botulinum toxin type A within three months prior to study enrollment |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Catholic University Saint Paul's Hospital; National Health Insurance Corporation Ilsan Hospital | Seoul |
Lead Sponsor | Collaborator |
---|---|
Catholic University of Korea Saint Paul's Hospital | Medy-Tox, National Health Insurance Service Ilsan Hospital |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual analogue scale | 4 weeks after intervention | No |
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