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Corneal Staining and Physiological Compromise After Eight Hours of Soft Contact Lens Wear

NCT01015768 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2020-09-18

Study results available
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Summary

The purpose of this study is to assess corneal staining and to measure the relative corneal epithelial "barrier" function (the degree to which the cornea can prevent penetration of colored sodium fluorescein dye into the eye) after 8 hours of wear with a known soft contact lens and multipurpose lens care solution combination.

Conditions

  • Contact Lens-induced Corneal Fluorescein Staining

Interventions

DEVICE

ReNu Multiplus multipurpose disinfecting solution

A new lens (PureVision) soaked 6 hours to overnight in ReNu Multiplus

DEVICE

Control

A new lens (PureVision) is soaked for two hours in non-preserved saline

Sponsors & Collaborators

  • Southern California College of Optometry at Marshall B. Ketchum University

    lead OTHER

Principal Investigators

  • Jerry R Paugh, OD, PhD · Southern California College of Optometry at Marshall B. Ketchum University

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
TRIPLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2010-01-31
Completion
2010-01-31

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 NCT01015768 on ClinicalTrials.gov