Clinical Trials Directory

Trials / Completed

CompletedNCT02522416

A Comparison of Two Devices for Measuring the Central Thickness of the Cornea Before and After Surgery (CECOT)

Status
Completed
Phase
Study type
Observational
Enrollment
50 (actual)
Sponsor
Fondation Ophtalmologique Adolphe de Rothschild · Network
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Corneal topography allows the measure of the radii of curvature and of the thickness of the cornea. It is essential for diagnosis in ophthalmology and allows to highlight corneal irregularities such as a keratoconus, or too thin corneas which are a contra-indication for laser refractive surgery. Several types of corneal topographers are commercially available. Some as the Orbscan(r), operate by analyzing the image of the patterns of a Placido disk associated with a light slit, allowing the collection of thousands of points of the anterior and posterior surface of the cornea. More recent systems such as the Pentacam(r) are based on automatic rotary cameras which capture images of the whole anterior segment of the eye. The aim of this study is to compare two topographs, the Pentacam(r) and the Orbscan(r) and, more specifically, the central corneal pachymetry measurements measured pre- and postoperatively.

Conditions

Interventions

TypeNameDescription
DEVICECentral corneal thickness measurement

Timeline

Start date
2015-11-30
Primary completion
2017-01-30
Completion
2017-03-15
First posted
2015-08-13
Last updated
2017-03-20

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02522416. Inclusion in this directory is not an endorsement.