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Objective Testing of Tear Film Stability

NCT00789529 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2013-05-31

Study results available
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Summary

The purpose of this study is to evaluate the in-vivo wettability of soft contact lenses when cared with two different multi-purpose solutions over a two week wearing period.

Conditions

  • Contact Lens Solutions

Interventions

DEVICE

Opti-Free® RepleniSH® MPDS

soft contact lens disinfecting solution

DEVICE

ReNu MultiPlus®

soft contact lens disinfecting solution

Sponsors & Collaborators

  • Alcon Research

    collaborator INDUSTRY

  • Manhattan Vision Associates

    lead OTHER

Principal Investigators

  • George Zikos, OS, MS · MVA/IVR

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-09-30
Primary Completion
2008-11-30
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 NCT00789529 on ClinicalTrials.gov