Glaucoma Trial, Recruiting NCT07322965 Sponsor: Institut Catala de Retina Condition: Glaucoma
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Glaucoma Trial, Recruiting

NCT07322965
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:

  • You have been diagnosed with chronic glaucoma (any type) in at least one eye, with confirmed damage to the structure of the eye shown by imaging tests.
  • Your glaucoma has also caused measurable loss in your field of vision, detected through a standard visual field test.
  • You have had at least 4 reliable visual field tests done before joining the study.
  • You are between 50 and 75 years old.
  • If both of your eyes are affected, the eye with the worse vision loss would be the one studied.

Who may not be able to join:

  • You have taken any vitamin or nutritional supplement in the month before screening.
  • You have a neurological condition, a retinal disease, significant cataracts, or take a medication called Pregabalin (Lyrica), as these can affect visual field test results.
  • You have a known allergy or sensitivity to aspirin, due to a possible related reaction with one of the study treatments (confirm with trial site).
  • You have had eye surgery or laser treatment on your eye in the 3 months before joining, or have any planned during the study.
  • Your visual field loss is either very mild or very severe, falling outside a specific range on a standard measurement scale (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.

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

Phone: +34 93 4340553

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
Institut Catala de Retina
Registry
ClinicalTrials.gov
Start date
1 April 2025
Est. completion
30 April 2027

Where this trial is recruiting

🇪🇸 Spain

Primary endpoints

Change from baseline in visual function assessed by Mean Deviation (MD) at 12 months; Change from baseline in visual function assessed by Visual Field Index (VFI) at 12 months

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