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Correlation Between Postoperative Central Corneal Thickness and Endothelial Damage After Cataract Surgery

Correlation Between Postoperative Central Corneal Thickness and Endothelial Damage After Cataract Surgery by Phacoemulsification

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03972670
Acronym
ECOCHI
Enrollment
85
Registered
2019-06-04
Start date
2014-08-01
Completion date
2018-01-01
Last updated
2019-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cataract, Phacoemulsification

Brief summary

To study correlation between postoperative corneal edema and endothelial cell loss after cataract surgery by microcoaxial phacoemulsification.

Detailed description

Cataract surgery facilitates improved visual acuity through extraction of an opacified lens, followed by intraocular lens implantation. An average adult cornea has 2000 to 2500 cells/mm2, a count that diminishes with age with a rate of attrition of approximately 0.3% to 0.5% per year. Long-term postoperative corneal transparency depends on the morphological stability and functional integrity of the corneal endothelium. It is well established that all surgical interventions that require entry into the anterior chamber result in some damage to the corneal endothelium. Endothelial cell loss results in cell hypertrophy to maintain continuity, resulting in a change in endothelium cell density and morphology. Many studies have assessed the impact of various surgical techniques on endothelial damage and numerous studies have investigated the factors influencing endothelial cell loss after phacoemulsification. The goal of this study is to investigate the correlation of postoperative corneal edema with the reduction of endothelial corneal cell density after phacoemulsification.

Interventions

None listed

Sponsors

Centre Hospitalier Régional Metz-Thionville
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* The presence of senile cataract with equivalent grades and a history of visual acuity regression

Exclusion criteria

* Patient with total white cataract * With history of ocular surgery * With other eye diseases (corneal pathology, Fuchs dystrophy, uveitis and glaucoma) or systemic diseases (diabetic disorder and dementia)

Design outcomes

Primary

MeasureTime frameDescription
PachymetryDay 1Measurement of the thickness of the eye's cornea with a pachymeter

Secondary

MeasureTime frameDescription
Endothelial cell densityDay 1Endothelial cell density measurements with noncontact specular microscope
Pachymetry after 1 monthDay 30Measurement of the thickness of the eye's cornea with a pachymeter
Endothelial cell density after 1 monthDay 30Endothelial cell density measurements with noncontact specular microscope

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026