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

Hospital Hietzing

Status: Completed

Conditions: Pseudophakia; Pseudoexfoliation Syndrome; Cataract

Treatments: Other: no intervention

Study type: Observational

Funder types: Other

Identifiers

NCT03453827

PEX Study

Details and patient eligibility

About

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.

Full 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.

Enrollment: 37 patients

Sex: All

Ages: 18 to 125 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• patients 4-6 years after standard cataract surgery
• pseudoexfoliation Syndrome (PES)

Exclusion criteria

• Diabetic retinopathy
• Age related macula Degeneration
• retinal bloodvessel disease

Trial design

37 participants in 2 patient groups

PEX

Description:

Patients after Cataract surgery with PES

Treatment:

Other: no intervention

Control

Description:

Patients after Cataract surgery without PES

Treatment:

Other: no intervention