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Time Study for Biometry Measurements With the Lenstar and IntraOcularLens (IOL) Master 500

NCT01550939 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 61

Last updated 2012-08-01

No results posted yet for this study

Summary

The objectives of this study are to determine the time needed to complete a full set of measurements (Total Ophthalmic Exam, Subject Data Entry and Acquisition of the Measurement) by each test device, the Lenstar 900 Version i4 and IOL Master 500.

Conditions

  • Pseudoaphakia

Interventions

DEVICE

Ophthalmic Biometer

One complete biometry examination

Sponsors & Collaborators

  • Haag Streit USA

    lead INDUSTRY

Principal Investigators

  • Michael E. Snyder, MD · Cincinnati Eye Institute

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2012-03-31
Completion
2012-03-31

Countries

  • United States

Study Locations

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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 NCT01550939 on ClinicalTrials.gov