Epidural Stimulation for Spinal Cord Injury

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study will evaluate a method to optimize parameter settings in epidural spinal cord stimulation used to recover lower extremity volitional movement. The study will also characterize improvement in autonomic function (such as blood pressure control) and other functions related to spinal cord injury.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 22
Healthy Volunteers: f
View:

• 22 years of age or older

• Able to undergo the informed consent/assent process

• Stable, motor-complete paraplegia

• Discrete spinal cord injury between C6 and T10

• ASIA A or B Spinal Cord Injury Classification

• Medically stable in the judgement of the principal investigator

• Intact segmental reflexes below the lesion of injury

• Greater than 1 year since initial injury and at least 6 months from any required spinal instrumentation

• Willing to attend all scheduled appointments

Locations
United States
Minnesota
Hennepin County Medical Center
RECRUITING
Minneapolis
Contact Information
Primary
Study Coordinator
estand@umn.edu
612-873-9113
Backup
David Darrow, MD MPH
estand@umn.edu
612-217-4290
Time Frame
Start Date: 2017-08-07
Estimated Completion Date: 2028-01
Participants
Target number of participants: 100
Treatments
Experimental: Epidural Spinal Cord Stimulation
Epidural Spinal Cord Stimulation
Related Therapeutic Areas
Sponsors
Collaborators: Hennepin Healthcare Research Institute, Minnesota Office of Higher Education, Minneapolis Veterans Affairs Medical Center, Hennepin County Medical Center, Minneapolis
Leads: University of Minnesota

This content was sourced from clinicaltrials.gov