Oxiplex gel is an investigational device, meaning it is not approved in the U.S. by the FDA. Oxiplex may help prevent some of the side effects that can occur after your lumbar spine surgery, such as residual leg pain, back pain, and neurological symptoms. The study is designed to examine the safety and efficacy of the device.
This study is currently enrolling.
Interested in participating?
Fill out the information below and we will reach out to you within two business days with more information on qualifications for this trial and how to participate.