Status:

COMPLETED

Refractive Outcomes After Cataract Surgery in Eyes With Pseudoexfoliation Syndrome

Lead Sponsor:

Medical University of Lublin

Conditions:

Refractive Errors

Cataract

Eligibility:

All Genders

18+ years

Brief Summary

To evaluate the refractive outcomes of cataract surgery in PEX syndrome and determine which of the commonly used IOL formulas (SRK/T, Barrett Universal II and Hill-RBF) is the best in predicting posto...

Detailed Description

The primary outcome measure was to compare refractive outcomes (MAE, MedAE, percentage of eyes within certain range of prediction error) in PEX and control eyes. The secondary outcome measure was to d...

Eligibility Criteria

Inclusion

  • senile cataract with/without PEX

Exclusion

  • corneal pathology
  • glaucoma,
  • corneal astigmatism greater than 2.0 diopters (D),
  • previous eye surgery or subjects with decreased vision due to other reasons than cataract (e.g., exudative age-related macular degeneration (AMD), proliferative diabetic retinopathy, inflammatory eye diseases),
  • intraoperative complications,
  • postoperative corrected distance visual acuity (CDVA) worse than 20/40,
  • axial length below 21 mm and above 25 mm,
  • dense cataracts or poor fixation requiring ultrasound biometry
  • eyes with manifest iridophacodonesis and those in which a capsular tension ring was inserted

Key Trial Info

Start Date :

October 1 2016

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

May 30 2018

Estimated Enrollment :

80 Patients enrolled

Trial Details

Trial ID

NCT04783909

Start Date

October 1 2016

End Date

May 30 2018

Last Update

March 5 2021

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