Clinical Trials Directory

Trials / Completed

CompletedNCT03453827

Long-term Intraocular Lens (IOL) Decentration and Tilt in Eyes With Pseudoexfoliation Syndrome (PES) Following Cataract Surgery

Assessment of Long-term Intraocular Lens (IOL) Decentration and Tilt in Eyes With Pseudoexfoliation Syndrome (PES) Following Cataract Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
37 (actual)
Sponsor
Hospital Hietzing · Academic / Other
Sex
All
Age
18 Years – 125 Years
Healthy volunteers

Summary

To evaluate long-term intraocular lens (IOL) decentration and tilt in eyes with pseudoexfoliation syndrome (PES) following cataract surgery using Visante anterior segment OCT and iTrace Visual Function Analyzer.

Detailed description

64 eyes following cataract surgery from 2009 to 2012 were included, 34 eyes had PES, 30 eyes did not show PES. A standard phacoemulsification procedure followed by IOL implantation was performed and patients were followed 4-6 years after surgery (mean=69 months). Best corrected visual acuity (BCVA), intraocular pressure (IOP) and capsulorhexis size were measured. IOL tilt and IOL decentration were evaluated using Visante Omni anterior segment OCT (Carl Zeiss Jena GmBH, Germany). The iTrace VFA (Visual Function Analyzer, Topcon Medical Systems, Inc.) was used to measure internal, corneal and total optical aberrations.

Conditions

Interventions

TypeNameDescription
OTHERno interventionno intervention

Timeline

Start date
2016-04-01
Primary completion
2017-04-28
Completion
2017-04-28
First posted
2018-03-05
Last updated
2018-03-08

Source: ClinicalTrials.gov record NCT03453827. Inclusion in this directory is not an endorsement.