This is a small study of 4 people to test the safety and possible therapeutic benefits of stimulating the spinal cord with 2 electrodes surgically implanted next to the spinal cord (Targeted Epidural Spinal Stimulation; TESS), on blood pressure management after spinal cord injury. If included, the participant will undergo surgery for implantation of the TESS device. Optimization of the device will be completed over one month, followed by 2 weeks of supervised at-home TESS testing over 5 sessions per week. Thereafter, the participant will have a minimum of 5 TESS sessions per week and 1 laboratory session each month, for up to 10 months.
Traumatic
Type
Details
• The participant will take part in 8 study phases, including screening and pre-implantation testing, • The participant will undergo surgery for implantation of the TESS device. • The device will be optimized over one month. • Supervised at-home TESS testing will be performed for 2 weeks over 5 sessions per week. • Thereafter, the participant will have a minimum of 5 TESS sessions per week and 1 laboratory session each month, for up to 10 months. • Additional testing during a configuration of additional TESS programs.
Main benefits
General health
Additional benefits
Arm/hand function
Mental health and psychosocial factors
Sensory function
Spasticity
Standing/walking/mobility
Good to know: Potential benefits are defined as outcomes that are being measured during and/or after the trial.
Wings for Life has proudly initiated, led and funded the new version of the SCI Trials Finder website. Wings for Life aims to find a cure for spinal cord injuries. The not-for-profit foundation funds world-class scientific research and clinical trials around the globe.
Learn moreWings for Life has proudly initiated, led and funded the new version of the SCI Trials Finder website. Wings for Life aims to find a cure for spinal cord injuries. The not-for-profit foundation funds world-class scientific research and clinical trials around the globe.
Learn more