Hypertension 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 40 years old or older and have mild to moderate open-angle glaucoma that is not well controlled
- Your eye pressure is 18 mmHg or higher, even while using at least one eye drop medication to lower it
- Your eye examination shows an open drainage angle in the eye (confirmed by a special eye exam called gonioscopy)
- Your cornea (the clear front part of your eye) is clear and the surface of your eye is healthy
- You are able and willing to give your consent, take part in the trial, and attend follow-up appointments
- You have glaucoma-related vision field loss in one or both eyes, confirmed by at least two consistent vision tests
- The tissue on the surface of your eye (in the upper area) is healthy and movable
- Your best corrected vision is at least 20/100 (meaning you can see with glasses or contacts to a reasonable level)
- Your vision field loss is not worse than a certain level, and you do not have a specific pattern of central vision loss (confirm with trial site)
- You are not expected to need any other eye surgery (such as cataract surgery) within 3 months of joining the trial
Who may not be able to join:
- You have previously had glaucoma surgery (such as a trabeculectomy, shunt, or valve) in the area of the eye being treated
- You have a type of glaucoma caused by closed drainage angles, abnormal blood vessels, eye inflammation, or injury
- The surface of your eye in the treatment area has scarring, has had surgery before, or has other problems
- The white of your eye (sclera) in the treatment area is abnormally thin or has structural problems
- Your eye pressure is higher than 35 mmHg at your screening appointment
- You currently have an active eye infection or inflammation (such as eyelid, conjunctival, corneal, or internal eye inflammation)
- You have had abnormal new blood vessel growth in the iris (coloured part of the eye) in the past 6 months
- You have a problem with the drainage of blood vessels on the surface of your eye (confirm with trial site)
- You have a certain type of lens implant located at the front of your eye (anterior chamber intraocular lens)
- You have a bleeding disorder that is not controlled, or you are taking blood-thinning medication without proper management around the time of any procedure
- You have severe, advanced glaucoma damage to your optic nerve
- You have a specific corneal condition (Fuchs endothelial dystrophy) that is showing signs of the cornea breaking down
- The thickness of your cornea is greater than 600 μm (a measurement taken during an eye exam)
- You have a severe level of short-sightedness classified as pathological myopia
- You are not able to follow post-procedure care instructions or attend follow-up visits
- You are pregnant, breastfeeding, planning to become pregnant, or are of childbearing age and not using a reliable form of contraception (certain contraceptive methods must have been in use for a specific period before the study begins — confirm with trial site)
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: 6474533253
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 lowering
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.