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Evaluation of Corneal Staining With Various Contact Lens/Solution Combinations

NCT00381446 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2007-09-27

No results posted yet for this study

Summary

The purpose of this study is to quantify the amount of corneal staining observed with various marketed contact lens/multipurpose solution combinations. The hypothesis is that there are measurable differences in the amount of corneal staining between the various combinations.

Conditions

  • Corneal Epithelial Disruption
  • Corneal Staining

Interventions

DEVICE

Marketed contact lens care products

Sponsors & Collaborators

  • Alcon Research

    collaborator INDUSTRY

  • Andrasko, Gary, OD, LLC

    lead INDIV

Principal Investigators

  • Gary J. Andrasko, OD, MS

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-07-31
Completion
2008-03-31

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 NCT00381446 on ClinicalTrials.gov