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OpenTrials
Completed

NCT Number: NCT02781948

Evaluation of the Repeatability and Reproducibility of Corneal Epithelial Thickness Mapping With iVue SD-OCT

Evaluate the repeatability and reproducibility of iVue for measuring the total corneal thickness, the epithelial thickness, and the stromal thickness in normal subjects and patients with various corneal conditions.

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Key information

Conditions

Cornea Corneal Diseases Eye Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Normal

  • Able and willing to provide consent.
  • Able and willing to complete required exams. Corneal conditions
  • Able and willing to provide consent.
  • Able and willing to complete required exams.
  • History of refractive surgery, contact lens, dry eye or keratoconus.

Exclusion criteria

Normal

  • History of refractive surgery, contact lens, dry eye or pathology.
  • Blepharitis or meibomitis
  • Unable to complete required exams. Corneal conditions
  • Unable to complete required exams.

Treatment and study plan

optical coherence tomography

Device

Primary outcomes

  1. Epithelial thickness

    Time frame: Day 1

Secondary outcomes

  1. Corneal thickness

    Time frame: Day 1

Other outcomes

  1. Stromal thickness

    Time frame: Day 1

Sponsors and collaborators

Lead sponsor

Optovue

Industry

Registry information

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
May 25, 2016
Registry last updated
Sep 27, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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