Diagnostic Evaluation of the Tear Film

NCT00761917 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 229

Last updated 2015-03-31

No results posted yet for this study

Summary

The objectives of this study are to assess for a difference between normal and dry eye subjects in tear film quality using a diagnostic interferometry device and to determine whether there are associations between tear film quality and dry eye symptoms and signs.

Conditions

  • Dry Eye Syndromes

Interventions

DEVICE

Tear Film Analyzer

tear film images

Sponsors & Collaborators

  • TearScience, Inc.

    lead INDUSTRY

Principal Investigators

  • Christy Stevens, OD · Kolis Scientific

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-06-30
Primary Completion
2008-10-31
Completion
2008-11-30

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 NCT00761917 on ClinicalTrials.gov