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Distinguishing Healthy and Keratoconic Eyes Using Ultrahigh-Resolution OCT

Completed
Conditions
Keratoconus
Registration Number
NCT03184610
Lead Sponsor
Medical University of Vienna
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Age>18
  • Existence of Keratoconus
  • written informed consent obtained
Exclusion Criteria
  • Earlier surgery such as PK, CXL, relaxing incisions
  • Systemic diseases

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Corneal Epithelium ThicknessOne visit

Parameters collected from epithelium thickness data and maps

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Medical University of Vienna, Department of Ophthalmology

🇦🇹

Vienna, Austria

Medical University of Vienna, Department of Ophthalmology
🇦🇹Vienna, Austria

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