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Defining the Conjunctival Staining Method: Instillation Volume and Time Course to Assess Staining With Lissamine Green

NCT00768898 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2012-04-13

Study results available
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Summary

The purpose of this study is to determine the correct volume of lissamine green to use when assessing conjunctival staining, and to determine the time course needed to evaluate conjunctival staining after lissamine green has been instilled in the eye.

Conditions

  • Conjunctival Staining

Interventions

OTHER

2.5/5.0/10.0 µL lissamine green

vital stain solution

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-08-31
Primary Completion
2008-09-30

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 NCT00768898 on ClinicalTrials.gov