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Assessment of Corneal Endothelial Function Following Hypoxic Stress

Assessment of Corneal Endothelial Function Following Hypoxic Stress

Status
Withdrawn
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04175938
Enrollment
0
Registered
2019-11-25
Start date
2025-12-01
Completion date
2027-11-30
Last updated
2026-03-02

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

Conditions

Fuchs' Endothelial Corneal Dystrophy

Keywords

Fuch's Dystrophy, FECD, Fuch's Endothelial Corneal Dystrophy

Brief summary

The purpose of this study is to determine the difference in the cornea's response to contact lens placement between healthy and unhealthy eyes. The amount of corneal swelling (corneal thickness) between normal and FECD patients before and after a stress test will be measured and compared.

Detailed description

Clarity of the cornea is essential for optimal vision. The endothelium is a layer within the cornea that controls its clarity. Fuchs endothelial corneal dystrophy (FECD) is a progressive disease that affects both eyes in which the endothelium is dysfunctional, causing the cornea to swell and lose its clarity. Because of the vision loss associated with this swelling, corneal transplantation is needed for patients with advanced FECD. Currently, there is no method to directly measure how well endothelium cells are functioning in patients with FECD. Such a measurement, if it were possible, would allow physicians to identify patients who are at a higher risk of corneal swelling. The goal of this study is to establish a tool to measure and compare the amounts of corneal swelling between normal and FECD patients after a stress test is performed (the wearing of an FDA-approved contact lens.) Data will also be collected regarding how quickly and how well a cornea recovers from swelling in patients with healthy eyes compared to those with FECD.

Interventions

DEVICEWearing of contact lens

All subjects will wear a contact lens for three hours. The effect of the lens on the eye (epithelial swelling) will be measured at intervals after the lens is removed.

Sponsors

Massachusetts Eye and Ear Infirmary
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

A stress test will be performed (the wearing of a contact lens) to induce swelling in two groups: group A where the subjects have a diagnosis of Fuch's Endothelial Corneal Dystrophy, and group B where subjects have healthy eyes. Once the contact lens is removed, the cornea swelling will be measured in each group. The length of time it takes for the cornea to recover after being swollen will also be compared between the two groups.

Eligibility

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

Inclusion criteria

Subjects in the Fuch's Dystrophy arm of the study must meet following criteria: * Have a clinical diagnosis of Fuchs endothelial corneal dystrophy * Be scheduled for corneal transplantation in the next 6 months * Have no history of prior ocular surgery in study eye * Have no history of contact lens intolerance * Be motivated and willing to complete ocular imaging tests Subjects in the healthy eyes arm of the study must meet following criteria: * Have no prior history of ocular disease including ocular surface disease or glaucoma * Have no history of prior ocular surgery in study eye * Have no history of contact lens intolerance * Be motivated and willing to complete ocular imaging tests

Exclusion criteria

Pregnant women \-

Design outcomes

Primary

MeasureTime frameDescription
Thickness of the cornea before and after the stress testseven hoursMaximum changes in the thickness of the cornea measured before and after the stress test
The rate of corneal recovery after the stress testthree hoursThe extent of swelling evident at regular intervals during the 3 hours after the stress test
Time to full recovery from swellingthree hoursThe time it takes for the eye to no longer be swollen

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORUla Jurkunas, MD

Massachusetts Eye and Ear

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026