Electrical Stimulation for the Treatment of Glaucoma

Exclusion Criteria

• •1. Participant is unable to comply with study procedures or follow-up visits.
• •2. Participant has a history of ocular herpes zoster.
• •3. Participant has pathological nystagmus
• •4. Participant has evidence of visually significant retinopathy including but not limited to Diabetic retinopathy or retinitis pigmentosa.
• •5. Participant has evidence of corneal opacification or lack of optical clarity.
• •6. Participant has uveitis or other ocular inflammatory disease.
• •7. Participant has any electric or electronic implants such as a pacemaker.
• •8. Participant has acute conjunctivitis.
• •9. Participant has acute autoimmune disease.
• •10. Participant is currently participating in or has within the last 3 months participated in any other clinical trial of a drug by ocular (if in the study eye) or systemic administration.
• •11. Participant is pregnant or lactating.
• •12. Participant has, in the opinion of the investigator, any physical or mental condition that would increase the risk of participation in the study or may interfere with the study procedures, evaluations and outcome assessments. Including but not limited to all forms of dementia.
• •13. Unresected brain tumors
• •14. Implanted intracranial magnetic metals (metallic implants in the head / skull such as clamps, coils, ventriculo-peritoneal shunts, endoprostheses, etc.), which are not MRI-compatible. Note: metallic dental implants and titanium screws or plates are acceptable
• •15. Patients with any skin damage.
• •16. Children and comatose patients.
• •17. Patients with history of epileptic seizure within the last 10 years.
• •18. Patients with uncontrolled systemic hypertension or uncontrolled diabetes.
• •19. Self-reported alcohol or illicit drug addictions within the last 12 months.
• •20. Participant is not able to travel, to comply with the requirements of the study or not willing to complete the schedule of events (SOE) and/or unable to confirm follow-up participation
• •21. Prior participation in a vision training/stimulation study in the last 12 months