JPRN-jRCT1042220093
Recruiting
未知
Study of Efficacy of Spinal Cord DTM Stimulation via a Paddle-type Lead for Neuropathic Pain Following a Spinal Cord Lesion
Saito Ryuta0 sites10 target enrollmentNovember 21, 2022
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- europathic pain following a spinal cord lesion
- Sponsor
- Saito Ryuta
- Enrollment
- 10
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients with intractable neuropathic pain following spinal cord lesion resistance to medication treatments
- •\-18 years of age or older
- •\-Pain scale of VAS (Visual analog scale) is more than 4 point
- •\-Patients who classified as Frankel grade: B\-E
- •\-Patients in whom a paddle\-shaped lead can be placed on the rostral side of the spinal cord lesion
- •\-Patients who have obtained written consent from the patient
Exclusion Criteria
- •\-Patients for whom local and general anesthesia cannot be performed
- •\-Patients who classified as Frankel grade A
- •\-Patients receiving anti\-cancer therapy
- •\-Patients with a history of drug abuse
- •\-Patients with high risk of surgery, such as patients with unstable angina pectoris and with end\-stage liver disease presenting with hepatic encephalopathy
- •\-Patients with diabetes mellitus who are not well controlled (HbA1c 9% or more)
- •\-Patients with serious complications (liver disease, kidney disease, heart disease, lung disease, blood disease, brain disease, etc.)
- •\-Pregnant or potentially pregnant patients
- •\-Patients who are considered as inappropriate by a head of research or research assignations
Outcomes
Primary Outcomes
Not specified
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