A Study to Test the SENSE Device in Military-Age Patients With Traumatic Brain Injury

Exclusion Criteria

• •All subjects meeting any of the following criteria will be excluded from this study:
• •* Female patients who are pregnant or lactating.
• •* Known history of seizure or clinical seizure prior to initiating SENSE monitoring.
• •* Open skull fracture.
• •* Metallic intracranial clip, coil, or device (such as metallic ICP monitor).
• •* Presence or history of any other condition or finding that, in the investigator's opinion, makes the patient unsuitable as a candidate for the SENSE device monitoring or study participation or may confound the outcome of the study.
• •* Planned placement of an intraventricular catheter after the diagnostic (pre-enrollment) CT.
• •* Planned withdrawal of care within 24 hours of enrollment.
• •* Planned intracranial surgery within 24 hours of enrollment.
• •* Current participation in a medical or surgical interventional clinical trial.
• •* Planned or current use of continuous EEG monitoring.
• •* Control subjects with normal brain health will have no known history of seizure, stroke, brain tumor, TBI