Epithelial Thickness Map

Keratoconus Clinical Trial

Official title:

Comparison of Two Optical Coherence Tomography Devices in Corneal Epithelial Thickness Maps

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04578184
• Other study ID #: Epithelial thickness map
• Status: Recruiting
• Phase: N/A
• Start date: October 15, 2020
• Est. completion date: March 2021

Study information

• Verified date: October 2020
• Source: Vienna Institute for Research in Ocular Surgery
• Contact: Oliver Findl, Prof., MD
• Phone: +43 1 91021-84611
• Email: hkh.augen.abt[@]wgkk.at
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In keratoconic eyes, the corneal epithelium shows a localized thinning over the cone that is surrounded by an annulus of epithelial thickening. It has been postulated that epithelial thickness mapping can be a sensitive tool for the keratoconus diagnosis. In keratoconus screening the 5 mm diameter of the corneal centrum may be sufficient while studies have shown that the cone apex is located in this area.

Aim of this study is to assess agreement and repeatability of epithelial thickness measurements using two optical coherence tomography devices in healthy and keratoconus corneas.

Secondary objective is to evaluate the differences between healthy and keratoconus eyes using epithelial thickness map data.

This is a prospective monocentric study that includes patients divided into two groups:

patients with keratoconus and a control group formed out of patients without corneal pathologies. For each patient only one eye will be included and corneal measurements will be performed, focused on the corneal epithelium thickness.

Description:

In total 50 eyes of 50 patients will be included, divided into two groups: study group comprised of 20 eyes with diagnosed keratoconus and a control group formed out of 30 healthy eyes.

Patients included in the study will be measured with the corneal acquisition mode, also allowing for epithelium thickness data, on each device without pupil dilatation. After each measurement patients will be asked to blink in order to allow adequate tear-film recovery. Each patient will be measured three times with both devices. Only one visit will be necessary.

The order in which the measurements will be performed (Anterion or MS-39) will be randomised using randomised.org.

The corneal epithelial thickness will be measured as the distance between the air-tear and the epithelium-Bowman interfaces.

Main outcome variable:

• Mean differences in central corneal epithelial thickness between the devices investigated (+ limits of agreement (1.96xSD) between the investigated devices)

Secondary outcome variables:

• Repeatability coefficient (within subject standard deviation - SD) and coefficient of variation of the two devices

• Comparison in epithelial thickness between normal and keratoconus eyes

• Sensitivity and specificity of swept-source OCT device in keratoconus diagnosis

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 50
• Est. completion date: March 2021
• Est. primary completion date: February 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 21 Years to 100 Years

Eligibility

Inclusion Criteria:

• Patient with diagnosed keratoconus (diagnosed using tomography and topography map changes and slit-lamp changes) and patients with healthy cornea

• Age 21 and older

• Signed informed consent

Exclusion Criteria:

• Previous ocular surgery

• Associated corneal pathologies (e.g. trauma, edema, scarring)

• In women of childbearing age, a pregnancy test will be performed before inclusion into the study.

Related Conditions & MeSH terms

• Keratoconus

Intervention

Diagnostic Test:
• Corneal epithelial thickness measurements
Corneal epithelial thickness measurements using two optical coherence tomography devices in healthy and keratoconus corneas.

Locations

Country	Name	City	State
Austria	Hanusch Hospital, Ophthalmology Department	Vienna

Sponsors (1)

Lead Sponsor	Collaborator
Vienna Institute for Research in Ocular Surgery

Country where clinical trial is conducted

Austria, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Agreement between two ss-OCT devices in corneal epithelial thickness measurements (LoA in micrometer)		6 months
Secondary	Repeatability between two ss-OCT devices in corneal epithelial thickness measurements (determination of within-subject standard deviation and Coefficient of variation)		6 months