DoD AtMS for Posttraumatic Peripheral Neuropathic Pain

Who May Qualify: - Veterans (men or women) of any race or ethnicity who are at least 18 years of age - Chronic peripheral neuropathic pain present for more than 4 months after a traumatic or surgical event per medical history - Have an average daily Numerical Pain Rating Scale (NPRS) score \> 3 - At least one negative or positive sensory sign or symptom confined to innervation territory of the lesioned nervous structure - Prior diagnostic tests confirming lesion or disease explaining neuropathic Who Should NOT Join This Trial: - Pregnancy - Subjects with central neuropathic pain (ex: due to diabetic peripheral neuropathy, HIV, chemo/anti-viral therapy, carpal tunnel syndrome, post-traumatic pain classified as central rather than peripheral) - Subjects with pain due to Complex Regional Pain Syndrome - Phantom limb pain after amputation (stump pain and phantom sensation are allowed) - Subjects with skin conditions in the affected dermatome - Subjects with other pain such as lumbar or cervical radiculopathy that may confound assessment - Any subject considered at risk of suicide - Use of prohibited medications in the absence of appropriate waiting period after previous treatments - Participation in any other clinical trial within the 30 days prior to screening and/or during participation in this study - Heart pacemaker - Subjects with a current diagnosis of DSM-IV-TR Axis I disorder (GAD \& MDD are allowed if clinically stable) - Subjects with pending lawsuits related to injury - Subjects who have previously received either transcranial or transcutaneous magnetic stimulation therapy in the past Always talk to your doctor about whether this trial is right for you.