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Comparative Study of the Optical Biometer for Measurements of the Eye

NCT01729962 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 125

Last updated 2013-06-28

No results posted yet for this study

Summary

The primary purpose of this comparative clinical study is to collect clinical data to demonstrate the equivalence of the investigational device to the predicate device for measurements of the eye. The secondary purpose is to evaluate any adverse events that occur during the clinical study.

Conditions

  • Normal Non-fluency
  • Cataract
  • Aphakic Eye
  • Eyes With Corneal Abnormality

Sponsors & Collaborators

  • Nidek Co. LTD.

    lead INDUSTRY

Principal Investigators

  • Karl G Stonecipher, M.D. · Physicians Protocol

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-12-31
Primary Completion
2013-04-30
Completion
2013-05-31

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 NCT01729962 on ClinicalTrials.gov