MedTrace Logo

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

NCT02377154 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2017-12-13

No results posted yet for this study

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

  • Healthy

Interventions

DEVICE

Slit lamp

Examination of cornea

DEVICE

Autorefractor

Measurement of refraction

DEVICE

IOLMaster 500

Measurement of axial length and white-to-white distance; Keratometry; IOL calculation

DEVICE

Pentacam HR

Measurement of white-to-white distance; Keratometry

DEVICE

LenStar LS900

Measurement of axial length and white-to-white distance; Keratometry; IOL calculation

DEVICE

VERION Image Guided System

Measurement of white-to-white distance; Keratometry; IOL calculation with axial length value of IOLMaster 500

Sponsors & Collaborators

  • Heidelberg University

    lead OTHER

Principal Investigators

  • Mike P Holzer, MD, FEBO · Department of opthalmology, University of Heidelberg

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-02-28
Primary Completion
2015-05-31
Completion
2016-05-31

Countries

  • Germany

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02377154 on ClinicalTrials.gov