Clinical Trials Directory

Trials / Completed

CompletedNCT02377154

Comparability of Keratometry of VERION Image Guided System With Established Measuring Devices

Comparability of Keratometry and Intraocular Lens (IOL) Calculation of VERION Image Guided System With Established Measuring Devices in Ophthalmologically Healthy Individuals

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
150 (actual)
Sponsor
Heidelberg University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine if the keratometric functions of the VERION Image Guided System are comparable to those of established keratometric devices (IOLMaster 500, Pentacam HR, LenStar LS900). Calculated intraocular lenses (IOLs) are compared as a clinical consequence of the biometric measurement for IOLMaster 500, LenStar LS900 and VERION Image Guided System. In addition the comfort and duration of examination in the different devices is evaluated.

Conditions

Interventions

TypeNameDescription
DEVICESlit lampExamination of cornea
DEVICEAutorefractorMeasurement of refraction
DEVICEIOLMaster 500Measurement of axial length and white-to-white distance; Keratometry; IOL calculation
DEVICEPentacam HRMeasurement of white-to-white distance; Keratometry
DEVICELenStar LS900Measurement of axial length and white-to-white distance; Keratometry; IOL calculation
DEVICEVERION Image Guided SystemMeasurement of white-to-white distance; Keratometry; IOL calculation with axial length value of IOLMaster 500

Timeline

Start date
2015-02-01
Primary completion
2015-05-01
Completion
2016-05-01
First posted
2015-03-03
Last updated
2017-12-13

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT02377154. Inclusion in this directory is not an endorsement.