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 are willing and able to sign and date a consent form agreeing to take part in the study
- You are willing to follow all study procedures and be available for the full length of the study
- You are a man or woman between 18 and 99 years old
- You are in good enough general health to travel to and attend your appointment on the day of the study
Who may not be able to join:
- You are under 18 years old
- You are unable or unwilling to sign a consent form to take part in the study
- You have a condition that makes it difficult to get an accurate eye pressure reading, such as uncontrollable eye blinking (blepharospasm), involuntary eye movement (nystagmus), significant problems with the clear front surface of the eye (corneal pathology), or you wear contact lenses and cannot remove them for the appointment
- You have significant thinning of the white part of your eye (the sclera) (confirm with trial site)
- You have a known allergy to proparacaine (a numbing eye drop) or fluorescein (an eye dye), as both are used during the eye pressure measurement part of the study
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: 716-408-6909
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
Intraocular Pressure
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.