Biomedical Device Clinical Trial Shows Improvements for Spinal Cord Injuries

A group of four faculty members stand together at the UT Dallas Bioengineering Sciences Building.
The leadership group for the Texas Biomedical Device Center includes, from left, Dr. Michael Kilgard, professor of neuroscience and Margaret Fonde Jonsson Professor; Dr. Jane Wigginton, chief medical officer of the Texas Biomedical Device Center; Dr. Seth Hays, associate professor of bioengineering and Fellow, Eugene McDermott Distinguished Professor; and Dr. Robert Rennaker, professor of neuroscience and Texas Instruments Distinguished Chair in Bioengineering.

The unprecedented results position the UT Dallas scientists to proceed with a pivotal trial — the final hurdle on the road to potential Food and Drug Administration (FDA) approval of vagus nerve stimulation for treatment of upper-limb impairment due to spinal cord injury.

— Dr. Seth Hays, associate professor of bioengineering and Fellow, Eugene McDermott Distinguished Professor
in the Erik Jonsson School of Engineering and Computer Science

“In stroke, people who do only therapy may get better, and adding CLV multiplies that improvement,” he said. “This study is different: Therapy alone for spinal cord injury didn’t help our participants at all. It is truly groundbreaking that we’re creating a gain where there otherwise would be none.”

VNS device is positioned on a dime to show small scale.
The most recent wireless version of the closed-loop vagus nerve stimulation device is about the size of a dime.

The trial involved 19 participants with chronic, incomplete cervical spinal cord injury. Each person performed 12 weeks of therapy, playing simple video games to trigger specific upper-limb movements. The implant was activated upon successful movements, resulting in significant benefits for arm and hand strength.

“These activities allow patients to regain strength, speed, range of motion and hand function. They simplify daily living,” said Dr. Robert Rennaker, professor of neuroscience and the Texas Instruments Distinguished Chair in Bioengineering, who designed the miniature implanted CLV device.

The study served as both a Phase 1 and Phase 2 clinical trial and in its first phase, included randomized placebo control in which nine of the 19 participants received sham stimulation rather than active treatment during the first 18 therapy sessions, then received CLV in the latter 18 sessions. All 19 participants completed 36 sessions of intensive rehabilitation at a rate of approximately three per week.

The participants ranged in age from 21 to 65 and were from one to 45 years post-injury. Neither of those factors nor the severity of the impairment in those with any hand movement influenced the degree of response to treatment.

“This approach produces results regardless of these factors which often cause significant differences in success rates of other types of treatment,” said study co-author Dr. Jane Wigginton, medical doctor and chief medical officer at TxBDC, co-director of UTD’s Clinical and Translational Research Center and medical science research director at the Center for BrainHealth.

“It is remarkable from a medical standpoint,” said Wigginton, who planned the clinical interactions and patient protections for the trial.

TxBDC has worked to treat a wide variety of conditions using CLV across 13 years of research. As a result, the FDA has approved vagus nerve stimulation for treating impaired upper-limb movement in stroke patients.

Wigginton said the latest results are especially exciting because they help people for whom there is no other existing solution.