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 willing and able to give informed consent to take part
- People who have been clinically diagnosed with primary open angle glaucoma (a common type of glaucoma where the eye's drainage angle is open), including a type called normal tension glaucoma
- People who have been clinically diagnosed with ocular hypertension (higher than normal pressure inside the eye, without glaucoma damage)
- People whose eye drainage angles are confirmed as open on a specialist eye examination
- People aged 18 or older, of any gender
- People whose cornea (the clear front surface of the eye) measurements fall within a specific size range in the eye being studied (confirm with trial site)
- People whose corneal thickness in the study eye falls within a specific range — between 490 and 600 micrometres (confirm with trial site)
Who may not be able to join:
- People who have any eye condition other than glaucoma or ocular hypertension
- People who have previously had surgery or laser treatment for glaucoma, cataracts, or vision correction
- People who have an abnormality of the cornea or the white of the eye that would prevent wearing a contact lens
- People who have insufficient tear production (dry eye affecting the ability to wear contact lenses)
- People who have a known allergy to eye numbing drops (corneal anaesthetic)
- People who have a medical reason they cannot wear silicone contact lenses
- People who have a medical reason they cannot take the study medications — Diamox, Latanoprost, or Timolol (confirm with trial site)
- People who have skin irritation, eczema, or another condition that prevents wearing adhesive patches on the skin
- People who are unable or unwilling to follow the study procedures
- People who do not have the capacity to give informed consent
- People with a history of heart failure, a treated heart condition, or kidney failure
- People with known cognitive (thinking or memory) disorders
- People who are unable to follow study procedures for any reason, such as language difficulties, psychological conditions, or dementia
- People who are currently taking part in, or have taken part in, another clinical trial involving an experimental drug within the past 30 days
- The trial investigators themselves, their family members, employees, or anyone else in a dependent relationship with the investigator
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: Kaweh Mansouri, Pr, Swiss Glaucoma Foundation
Phone: +41 21 619 36 02
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
GF IOP measurement as compared to IOP
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.