Clinical trial Recruiting at 1 site Observational Ages 60 to 80

Assessing corneal properties in patients with pseudoexfoliation syndrome

Official title: A Comparative Study of Anterior Segment Structural Features, Biomechanical Behaviour and Optical Properties of the Cornea in Patients With and Without Pseudoexfoliation Syndrome.

Run by Aristotle University Of Thessaloniki · NCT06731530 · Data updated 2026-11-12

This study is testing how pseudoexfoliation syndrome affects the eye's surface and structure in people aged 60-80 compared to others without the condition.

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Quick facts

Study typeObservational
Ages60 Years to 80 Years
SexAll
Enrollment86 (estimated)
SponsorAristotle University Of Thessaloniki
Academic / other
Locations1 site (Thessaloniki)
StatusRecruiting
StartedDecember 13, 2024
Main results expectedMay 2025
Study endsMay 2025
Registry record updatedDecember 27, 2024
Trial IDNCT06731530 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals aged 60-80 with unilateral or bilateral pseudophakia and an open anterior chamber angle.

Probably not a fit

Patients with a history of intraocular surgery other than uncomplicated cataract surgery or those with significant ocular conditions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study evaluates the impact of pseudoexfoliation syndrome on corneal biomechanics, optical clarity, and anterior segment structural features. Patients aged 60-80 with pseudoexfoliation syndrome will undergo a series of examinations using advanced imaging technologies, including Pentacam-AXL and Corvis ST, to assess corneal optical properties and biomechanical parameters. The results will be compared to a control group of age-matched individuals without the syndrome to better understand the effects of this condition on the eye.

Why it matters

Potential benefit: If successful, this study could lead to improved diagnostic and treatment strategies for patients with pseudoexfoliation syndrome.

How similar studies have gone: While there have been studies on corneal properties, this specific approach focusing on pseudoexfoliation syndrome is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* age 60-80 years.
* unilateral or bilateral pseudophakia (cataract surgery undergone at Papageorgiou General Hospital, Thessaloniki, Greece).
* open anterior chamber angle (grade \> 2, van Herick method).

Exclusion Criteria:

* History of intraocular surgery other than uncomplicated cataract surgery (phakoemulsification).
* Cataract surgery within the last 3 months.
* History of ocular trauma.
* Use of contact lenses.
* Corneal pathology.
* Use of anti-VEGF medications.
* History of uveitis or active uveitis.
* Hypertension (IOP \> 21 mmHg) or glaucoma.
* Myopia or hyperopia greater than 3 diopters.
* Astigmatism greater than 1.5 diopters.
* Posterior capsular opacification grade 2, 3, or 4 based on the EPCO grading scale.
* Tear break-up time \<10 sec

Where it's running

  • 2nd Department of Ophthalmology, Papageorgiou General Hospital
    Thessaloniki, Greece
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.