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Clinical Trials/NCT05447130
NCT05447130
Completed
Not Applicable

Corneal Endothelial Evaluation After Phacoemulsification in Eyes With Pseudoexfoliation Syndrome

Minia University1 site in 1 country40 target enrollmentMarch 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Corneal Endothelial Cell Loss
Sponsor
Minia University
Enrollment
40
Locations
1
Primary Endpoint
corneal endothelial cell loss
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

To study corneal endothelial cells changes after phacoemulsification in patients with senile cataract and pseudoexfoliation syndrome (PEX) compared with control patients with senile cataract using specular microscope.

Detailed Description

In a prospective interventional case-control study, 20 eyes with cataract and PEX and 20 control eyes with cataract without PXE were subjected to phacoemulsification and posterior chamber foldable intraocular lens implantation in Minia University Hospital and Genaidy Eye Center between March 2019 and December 2020. Specular microscopy was done preoperatively, 3 and 6 months postoperatively. Endothelium cell density (ECD), coefficient variation (CV), hexagonality, pleomorphism and corneal thickness were evaluated and compares between PXE and control eyes.

Registry
clinicaltrials.gov
Start Date
March 1, 2019
End Date
December 31, 2020
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Minia University
Responsible Party
Principal Investigator
Principal Investigator

Hosny Ahmed Zein

Assistant Professor

Minia University

Eligibility Criteria

Inclusion Criteria

  • senile cataract age more than 55 years

Exclusion Criteria

  • PEX with glaucoma, eyes with cornea guttata or any corneal dystrophy, zonular dehiscence, very dense nuclear cataract (cataracta nigra) history of previous ocular surgery.

Outcomes

Primary Outcomes

corneal endothelial cell loss

Time Frame: 6 months

corneal endothelial cell loss

Study Sites (1)

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