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Distinguishing Healthy and Keratoconic Eyes Using Ultrahigh-Resolution OCT

NCT03184610 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2017-06-12

No results posted yet for this study

Summary

The OCT used in this trial offers the advantage of both a non-contact method and a very high axial resolution. Determined parameters with the highest potential of diagnostic discrimination between eyes with Keratoconus and healthy eyes are investigated. Aim of this trial is to investigate differences of specific parameters of epithelium thickness maps at healthy eyes and eyes with Keratoconus.

Conditions

  • Keratoconus

Interventions

DEVICE

OCT-scanning

All participants will be scanned with a OCT-device

Sponsors & Collaborators

  • Medical University of Vienna

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-12-31
Primary Completion
2017-06-30

Countries

  • Austria

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03184610 on ClinicalTrials.gov