A Study of Remote Electrical Neuromodulation for Acute Procedural Pain

Exclusion Criteria

• •Participants with an active implanted electrical and/or neurostimulator device (e.g., cardiac pacemaker, cochlear implant).
• •Participants with congestive heart failure (CHF), severe cardiac or cerebrovascular disease.
• •Participants with uncontrolled epilepsy.
• •Pregnant, trying to get pregnant or breastfeeding female participants.
• •Subjects participating in any other interventional clinical study.
• •Participants with other significant pain, medical or psychological problems that in the opinion of the investigator may confound the study assessments.
• •Participants who have previous experience with the device.
• •Patients with cranial deformities, prior cranial surgeries with violation of the calvarium, or shunt placement.
• •Patients receiving concurrent nerve blocks or trigger point injections within the same visit