Glaucoma Trial, Recruiting NCT07592988 Sponsor: Kazakh Eye Research Institute Condition: Glaucoma
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Glaucoma Trial, Recruiting

NCT07592988
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 have been diagnosed with glaucoma
  • People aged 18 years or older
  • People whose glaucoma is not adequately controlled with current eye medications
  • People for whom a doctor has decided that a specific laser treatment (called MP-CPC Laser) is the appropriate course of action

Who may not be able to join:

  • People under the age of 18
  • People who are unable or unwilling to give their formal written consent to take part in the study
  • People who may not be available to attend follow-up appointments during the study
  • People who have significant thinning of the white outer wall of the eye (confirm with trial site)
  • People who have had an eye infection, eye inflammation, or eye surgery in the eye being studied within the 2 months before enrolling
  • People with albinism who have no pigmentation (colouring) in the iris of the eye

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 15 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: Assiya Shaikenova, MD, Kazakh Eye Research Institute

Phone: +77055689966

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
Kazakh Eye Research Institute
Registry
ClinicalTrials.gov
Start date
18 May 2026
Est. completion
18 August 2026

Where this trial is recruiting

🇰🇿 Kazakhstan

Primary endpoints

Association Between Changes in Tear Fluid Interleukin Levels and Intraocular Pressure Reduction

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: 15 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