Glaucoma Trial, Recruiting NCT04024293 Sponsor: Sensimed AG Condition: Glaucoma
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Glaucoma Trial, Recruiting

NCT04024293
Recruiting Not Applicable

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Sensimed AG
Registry
ClinicalTrials.gov
Start date
1 October 2025
Est. completion
1 May 2026

Where this trial is recruiting

🇨🇭 Switzerland

Primary endpoints

GF IOP measurement as compared to IOP

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov