Clinical trial Recruiting at 1 site Interventional Ages 60 to 100

Comparing two methods for lens implantation in cataract surgery for patients with pseudoexfoliation syndrome

Official title: Outcome of Two Surgical Methods for IOLImplantation in Eyes With Pseudoexfoliation Syndrome: Lens in the Bag-technique Versus Lens in the Ciliary Sulcus With Optic Capture Technique

Run by Medical University of Vienna · NCT06053554 · Data updated 2026-11-12

This study is testing two different ways to implant lenses during cataract surgery to see which method works better for people with pseudoexfoliation syndrome.

Quick facts

Study typeInterventional
Ages60 Years to 100 Years
SexAll
Enrollment120 (estimated)
SponsorMedical University of Vienna
Academic / other
Locations1 site (Vienna)
StatusRecruiting
StartedSeptember 18, 2023
Main results expectedMay 2030
Study endsAugust 2030
Registry record updatedOctober 24, 2023
Trial IDNCT06053554 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals aged 60 to 100 who require bilateral cataract surgery and have been diagnosed with pseudoexfoliation syndrome.

Probably not a fit

Patients with end-stage glaucoma, crystalline lens subluxation, or active inflammatory diseases of the eye 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 study aims to compare the surgical outcomes of two intraocular lens (IOL) implantation techniques in patients with cataracts and pseudoexfoliation syndrome. It is a prospective, intraindividual comparative study where each patient undergoes bilateral cataract surgery, with one eye receiving a 3-point IOL in the capsular bag and the other receiving a 3-point IOL haptics in the ciliary sulcus. The study will evaluate differences in lens tilt, decentration, and the frequency of capsular phimosis between the two methods. Highly experienced surgeons will perform the procedures using femtolaser technology to ensure precision.

Why it matters

Potential benefit: If successful, this study could lead to improved surgical outcomes and visual acuity for patients undergoing cataract surgery with pseudoexfoliation syndrome.

How similar studies have gone: While similar surgical techniques have been explored, this specific comparative approach in the context of pseudoexfoliation syndrome is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 60 - 100
* Necessity for bilateral cataract surgery with pseudoexfoliation syndrome
* willing to give informed consent and follow-up the duration of study

Exclusion Criteria:

* Endstage glaucoma
* Christalline lens sub/ luxation
* active inflammatory diseases of the eye

Where it's running

  • Medical University of Vienna
    Vienna, Austria
    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.