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Distinguishing Healthy and Keratoconic Eyes Using Ultrahigh-Resolution OCT

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Medical University of Vienna

Status

Completed

Conditions

Keratoconus

Treatments

Device: OCT-scanning

Study type

Observational

Funder types

Other

Identifiers

NCT03184610
1160/2014

Details and patient eligibility

About

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.

Enrollment

60 patients

Sex

All

Ages

18 to 99 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age>18
  • Existence of Keratoconus
  • written informed consent obtained

Exclusion criteria

  • Earlier surgery such as PK, CXL, relaxing incisions
  • Systemic diseases

Trial design

60 participants in 2 patient groups

OCT-scanning
Description:
Patients with Keratoconus are scanned with an OCT-Prototype
Treatment:
Device: OCT-scanning
OCT-scanning for volunteers
Description:
Volunteers with healthy eyes are scanned with an OCT-Prototype
Treatment:
Device: OCT-scanning

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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