CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 30 enrolled
Drug / intervention
ReNu Multiplus multipurpose disinfecting solution +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01015768
NCT01015768N/ACompleted
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Corneal Staining and Physiological Compromise After Eight Hours of Soft Contact Lens Wear

Southern California College of Optometry at Marshall B. Ketchum University·interventional·Posted Nov 18, 2009·Updated Sep 18, 2020

In Brief

A clinical study evaluating ReNu Multiplus multipurpose disinfecting solution and Control for Contact Lens-induced Corneal Fluorescein Staining. Completed, enrolled 30 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsContact Lens-induced Corneal Fluorescein Staining
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedNov 18, 2009
Enrollment StartOct 1, 2009
Primary CompletionJan 1, 2010
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 16.6 years ago

Interventions

ReNu Multiplus multipurpose disinfecting solutiondevice

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

Controldevice

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