Retrospective Digital Computer Analysis of Keratoconus Evolution - REDCAKE

Sponsor
University Hospital, Antwerp (Other)
Overall Status
Completed
CT.gov ID
NCT03235856
Collaborator
European Vision Institute Clinical Research Network (Other)
972
1
16
60.9

Study Details

Study Description

Brief Summary

The purpose of this study is to create a database of keratoconic eyes with two or more corneal topographies/tomographies, at least 5 months apart

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Title: Keratometry values such as K1, K2 and the angle between these two; Value and location of the thinnest corneal point; Pachymetry progression (radial change of pachymetry); IS value (i.e., ratio of average curvature in superior and inferior sections)

    Description:

    The primary endpoint is to obtain a database, containing at least two valid corneal biometry measurements (Scheimpflug) recorded at least 5 months apart, for a predetermined number of suitable keratoconus patients.

    These data will be used to create a personalized three-dimensional model of the cornea at each time point, which permits classifying corneas according to shape and stage, as well as assessing the influence of patient age, gender, family history and ophthalmic habits (e.g. eye rubbing) on keratoconus progression. Based on corneal changes over time, an estimate of the underlying biomechanical changes will be made. All these data will then be combined to develop software for automated keratoconus detection and progression risk assessment to help ophthalmologists decide when to perform crosslinking on their patients.

    The primary variables are the elevation parameters derived directly from the Scheimpflug measuring device export files, along with the demographic and medical information (if available).

    Time frame: 5 months

    Once a predictive model for keratoconus progression speed based on multiple measurements, this can be improved to make predictions based on a single measurement. Furthermore, the database obtained in this work will also be a valuable resource to analyse the variation in keratoconus shape, which may lead to an improved classification of keratoconus types

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    972 participants
    Observational Model:
    Other
    Time Perspective:
    Retrospective
    Official Title:
    Retrospective Digital Computer Analysis of Keratoconus Evolution - REDCAKE
    Actual Study Start Date :
    Sep 1, 2017
    Actual Primary Completion Date :
    Dec 31, 2018
    Actual Study Completion Date :
    Dec 31, 2018

    Arms and Interventions

    Arm Intervention/Treatment
    Keratoconus patients

    This study involves a retrospective analysis of data recorded during routine clinical follow-up of keratoconus patients. As such, the impact for the patient is minimal as no additional tests need to be performed

    Outcome Measures

    Primary Outcome Measures

    1. To obtain a database, containing at least two valid corneal Scheimpflug measurements recorded at least 5 months apart, of 1500 keratoconus patients. [5 months]

      These data will be used to create a personalized three-dimensional model of the cornea at each time point, which permits classifying corneas according to shape and stage, as well as assessing the influence of patient age, gender, family history and ophthalmic habits (e.g. eye rubbing) on keratoconus progression. Based on corneal changes over time, an estimate of the underlying biomechanical changes will be made.

    2. To develop software to automatically detect keratoconus and estimate the keratoconus progression speed [18 months]

      The data from Outcome 1 will be combined to develop software for automated keratoconus detection and progression risk assessment to help ophthalmologists decide when to perform cross-linking on their patients.

    Secondary Outcome Measures

    1. To improve the predictive model for keratoconus progression speed so it can work using only one single measurement [18 months]

      Once a predictive model for keratoconus progression speed based on multiple measurements, this can be improved to make predictions based on a single measurement.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    12 Years to 40 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Age between 12-40 years.

    • Clinically diagnosed mild or moderate keratoconus in one or both eyes

    • Two or more Scheimpflug measurements (type Pentacam HR, Pentacam AXL, Ziemer Galilei, CSO Sirius) of good technical quality, separated at least five months apart.

    Exclusion Criteria:
    • Corneal scarring present in both eyes.

    • Known corneal or retinal pathologies, apart from keratoconus

    • Known ocular procedures/ treatments (including crosslinking)

    • Known systemic diseases (e.g. diabetes, MS, HIV/AIDS, hypertension,…), except allergies

    • Change in contact lenses between measurements (e.g. start wearing lenses, change from corneal to scleral lenses, etc.)

    • Fluorescein drops instilled into the eye before Scheimpflug measurement.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Antwerp University Hospital Edegem Belgium 2650

    Sponsors and Collaborators

    • University Hospital, Antwerp
    • European Vision Institute Clinical Research Network

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Jos Rozema, Senior researcher, Dpt of Ophthalmology, University Hospital, Antwerp
    ClinicalTrials.gov Identifier:
    NCT03235856
    Other Study ID Numbers:
    • ECR-AS-2017-12
    First Posted:
    Aug 1, 2017
    Last Update Posted:
    Nov 3, 2020
    Last Verified:
    Nov 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 3, 2020