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:
- You must be older than 18 years of age
- You must have been diagnosed with a specific type of glaucoma called primary open-angle glaucoma
- You must be able to complete a standard eye test that checks your field of vision
- You must be able to understand and agree to take part in the research by giving your consent
Who may not be able to join:
- You have a type of glaucoma caused by another condition, or a different kind of optic nerve problem that is not glaucoma
- You have had eye surgery in the past, unless it was cataract surgery or a minor type of glaucoma surgery
- You have a significant cloudiness or blockage inside the eye that affects vision (confirm with trial site)
- You are currently pregnant
- You have a condition that causes seizures (fits)
- You have a pacemaker or any other device implanted inside your body
- You experience severe dizziness or have a condition that seriously affects your balance
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
Principal Investigator: Brennan Eadie, MD, PhD, FRCSC, Nova Scotia Health
Phone: 19029560601
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
Visual field point-wise threshold values; Global indices of visual field loss; Reliability Indices
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.