Task-specific Epidural Stimulation Study

NARecruitingINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

November 8, 2017

Primary Completion Date

December 30, 2024

Study Completion Date

December 30, 2024

Conditions
Spinal Cord Injuries
Interventions
DEVICE

Acute epidural stimulation for cardiovascular stability

Eligible participants will be implanted with 16-electrode epidural array and epidural stimulator in the spinal cord. Participants received mapping for cardiovascular stability.

DEVICE

Long Term Epidural Stimulation for Cardiovascular Stability

Participants undergo approximately 4 months of epidural stimulation for cardiovascular stability, daily.

DEVICE

Participants undergo approximately 4 months of epidural stimulation for voluntary movement.

Participants undergo approximately 4 months of epidural stimulation for voluntary movement 4-7 days weekly.

DEVICE

Long Term Epidural Stimulation for Cardiovascular Stability plus Stand Training

Participants undergo approximately 4 months of epidural stimulation for cardiovascular stability, daily. Standing in a body weight support (BWS) harness on a treadmill or standing in a standing frame with epidural stimulation for standing up to 5 days weekly.

DEVICE

Participants undergo approximately 4 months of epidural stimulation for voluntary movement plus stand training.

Participants undergo approximately 4 months of epidural stimulation for voluntary movement, 4-7 days weekly. Standing in a body weight support (BWS) harness on a treadmill or standing in a standing frame with epidural stimulation for standing up to 5 days weekly. Standing in a body weight support (BWS) harness on a treadmill or standing in a standing frame with epidural stimulation for standing up to 5 days weekly.

Trial Locations (1)

40202

RECRUITING

University of Louisville, Louisville

All Listed Sponsors
collaborator

Christopher Reeve Paralysis Foundation

OTHER

lead

University of Louisville

OTHER