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Clinical Trials/JPRN-jRCT1042220093
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.

Registry
who.int
Start Date
November 21, 2022
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Saito Ryuta

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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