Glaucoma Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are 18 years of age or older
- People who have been diagnosed with glaucoma, with vision test results (Humphrey Visual Field 24-2) showing a mean deviation between -22 dB and -5 dB and a Visual Field Index between 10% and 90%, with reliable test results at screening
- People whose two consecutive visual field tests at the start of the study show results that are close to each other (difference of less than 2 dB)
- People whose best corrected vision (with glasses or contact lenses if needed) is at or above a certain level (0.2) in the eye being considered for treatment
- If both eyes meet the study requirements, one eye will be chosen at random by computer for participation
- People whose eye pressure is considered stable in the opinion of the study doctor
- People who are able to follow the study schedule and complete all required visits and tasks
- People who are able to understand and sign a consent form (if vision makes reading difficult, the form will be read aloud in full)
- People whose eye scan (OCT imaging) shows measurable changes in specific layers of the retina or optic nerve area
Who may not be able to join:
- People with a history of herpes infection in the eye
- People with uncontrolled abnormal eye movement (pathological nystagmus)
- People with a retinal disease that affects their vision
- People with cloudiness of the cornea that affects their vision
- People with a cataract that affects their vision
- People with inflammation inside the eye (such as uveitis)
- People who have an implanted electronic device, such as a pacemaker
- People with a rheumatological or autoimmune disease
- People with a brain tumour or magnetic metal implants inside the skull
- People with a history of epilepsy
- People with skin lesions around the eye area
- People with significant anxiety, as measured by a score above 12 on the Geriatric Anxiety Scale
- People with a history of claustrophobia
- People who have taken part in another clinical trial within the past 3 months that involved medication or training that could affect the eyes
- People with physical or mental health conditions that may increase the risks of taking part or affect how well study assessments can be completed (for example, dementia)
- People who have previously received electrical stimulation treatment to the eye, or taken part in a visual training study, within the past 12 months
- People with uncontrolled high blood pressure or uncontrolled diabetes
- People who are pregnant or breastfeeding
- People with a history of brain surgery (including craniotomy or burr hole surgery), serious head injury, brain tumour, abnormal blood vessels in the brain, or other surgery inside the skull
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: +886 972653340
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in visual field mean deviation (MD) from baseline to post-treatment
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.