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Treatment of Pain and Autonomic Dysreflexia in Spinal Cord Injury With Deep Brain Stimulation

NCT02006433 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 4

Last updated 2020-10-08

No results posted yet for this study

Summary

The purpose of this research study is to determine if DBS is a feasible, safe and effective therapy for pain and autonomic dysreflexia after spinal cord injury.

Conditions

  • Pain
  • Autonomic Dysreflexia

Interventions

DEVICE

Deep Brain Stimulation

Local anesthesis, MRI and CT scan of the brain followed by implantation of the stimulation device

Sponsors & Collaborators

  • United States Department of Defense

    collaborator FED

  • Jonathan Jagid

    lead OTHER

Principal Investigators

  • Jonathan R Jagid, M.D. · University of Miami

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-12-31
Primary Completion
2017-09-30
Completion
2017-09-30
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02006433 on ClinicalTrials.gov