OCT Agreement and Crossed Precision Study

NCT02050880 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 119

Last updated 2014-09-29

No results posted yet for this study

Summary

The purpose of this study is to asses the agreement of the RS-3000 Lite and RS-3000 Advance to the RS-3000, assess the crossed precision of each study device and to assess the transference of a reference database from the RS-3000 to the RS-3000 Lite and to the RS-3000 Advance.

Conditions

  • Glaucoma
  • Retinal Disease
  • Corneal Disease

Sponsors & Collaborators

  • Nidek Co. LTD.

    lead INDUSTRY

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2014-06-30
Completion
2014-06-30

Countries

  • United States

Study Locations

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Entities

Diseases

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 NCT02050880 on ClinicalTrials.gov