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Validation of TearLab Osmometer - Human Factor Usability Report

NCT00731484 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 233

Last updated 2016-04-12

Study results available
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Summary

The objective of this study is to validate the performance of the OcuSense TearLab™ osmolarity test when performed in physician office laboratories (POL) by health care professionals using human tear fluid collected from volunteer subjects and contrived tear samples.

Conditions

  • Dry Eye Syndromes

Sponsors & Collaborators

  • TearLab Corporation

    lead INDUSTRY

Principal Investigators

  • Michael A Lemp, MD · Clinical Professor of Ophthalmology, Georgetown University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-07-31
Primary Completion
2009-03-31
Completion
2009-03-31

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 NCT00731484 on ClinicalTrials.gov