Traumatic Brain Injury Peripheral Nerve Study

The subject will complete participation in three groups evaluating different programming parameters. After surgery, each subject will be randomized to Group A or Group B. Group C will be completed in the middle followed by the alternate A/B Group. Crossover will occur at 3 week intervals until subjects complete all three groups. During this period, all subjects will receive a subject programmer that will only enable them to activate the "on and off" positions and adjust amplitude within the prescribed range.

After subjects have completed the three pre-defined groups they will select the most effective and comfortable setting continuation of the study. The pulse width and frequency parameters will be set to the optimal settings identified by the subject. Amplitude will be set at a level that produces comfortable paresthesia for the subject.

Subjects will return to the clinic for programming changes post system internalization at 3 weeks, 6 weeks, and 9 weeks. Subjects will receive a PET scan at the 3 and 9 week visit. Additional follow-up evaluations will occur at 12 weeks, 18 weeks, and 24 weeks.

Inclusion criteria

• Subjects able to provide informed consent to participate in the study;
• Subjects between the ages of 18 and 65;
• Subjects with clear evidence and/or documentation of mild traumatic brain injury as defined by the American Congress on Rehabilitation Medicine (1993):

• Closed head injury/trauma
• Score of 13-15 on the Glasgow Coma Scale
• Documented/witnessed loss of consciousness < 30 minutes post injury
• Post traumatic amnesia less than 24 hours post injury.
• Subjects 12 month post-injury with DSM IV diagnosis of Postconcussive Disorder Research Criteria (see Appendix A for detailed definition):

• Evidence from neuropsychological testing of difficulty in attention or memory
• Complaints, at baseline, of three or more postconcussive symptoms that have been present at least 3 months.
• Subject medication that is TBI-related has remained stable for at least 4 weeks prior to baseline data collection;
• Current medical options have been tried and documented without sufficient improvement in symptom control;
• Subject agrees not to add or increase any medication throughout the randomization period of the study;
• Subject is willing to cooperate with the study requirements.

Exclusion criteria

• Subject diagnosed with a terminal disease (ie. cancer, leukemia, or advanced stages of disease resulting in less than 12 months life expectancy);
• Subject currently participating in another clinical study;
• Subject with demand-type cardiac pacemakers, an infusion pump or any implantable device (ie. deep brain stimulators, spinal cord stimulators, CSF shunts, aneurism clip and cochlear implants) which may interfere with therapy;
• Subject with significant depression and/or other significant psychiatric/behavioral problems likely to interfere with study completion or result in addition distress to the subject as determined by a qualified Psychiatrist or psychologist;
• Subject with an existing medical condition that is likely to require repetitive MRI evaluation in the future (ie. epilepsy, stroke, acoustic neuroma, tumor);
• Subject with a history of open head trauma;
• Subject with visual, hearing or motor deficits that impair ability to complete neurocognitive testing;
• Subject with a history of moderate to severe TBI;
• Subject with post traumatic seizure disorder;
• Subject with history of learning disability and/or ADHD
• Subject with history of chronic headache syndrome prior to post-concussive disorder;
• Subject is not willing to maintain current TBI-related medication regimen;
• Female candidates of child bearing potential who are pregnant (confirmed by positive urine/blood pregnancy test), not using adequate contraception (ie. oral contraceptives, injectibles, implants, patches, condoms, barrier methods, spermicides, intrauterine devices, and sterilization), or nursing (lactating) a child.