Study of new stimulation for neuropathic pain following a spinal cord lesio

Not Applicable

Recruiting

• Conditions: europathic pain following a spinal cord lesion

• Registration Number: JPRN-jRCT1042220093
• Lead Sponsor: Saito Ryuta

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-11-21
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 10

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified