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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