Clinical Trials Directory

Trials / Completed

CompletedNCT01155726

The Effect of Masking on Subjective Results During Daily Disposable Contact Lens Studies

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
134 (actual)
Sponsor
CIBA VISION · Industry
Sex
All
Age
17 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to explore the effect of masking on subjective ratings for two daily disposable contact lenses.

Conditions

Interventions

TypeNameDescription
DEVICENelfilcon A contact lensCommercially marketed, soft, hydrogel contact lens for daily wear, daily disposable use. Blister pack label and lens packaging visible to participant. Lenses inserted and removed by participant.
DEVICENelfilcon A contact lens with comfort additive (DACP), unmaskedCommercially marketed, soft, hydrogel contact lens with comfort additive for daily wear, daily disposable use. Blister pack label and lens packaging visible to participant. Lenses and removed inserted by participant.
DEVICENelfilcon A contact lens with comfort additive (DACP), maskedCommercially marketed, soft, hydrogel contact lens for daily wear, daily disposable use. Blister pack label and packaging not visible to participant. Lenses inserted and removed by the investigator.
DEVICENelfilcon A contact lens with comfort additive (DACP), partially maskedCommercially marketed, soft, hydrogel contact lens for daily wear, daily disposable use. Lens name and manufacturer on blister pack label concealed from participant. Lenses inserted and removed by the participant.
DEVICEEtafilcon A contact lensCommercially marketed, soft, hydrogel contact lens for daily wear, daily disposable use. Blister pack label and lens packaging visible to participant. Lenses inserted and removed by participant.
DEVICEEtafilcon A contact lens with comfort additive (1DAVM), unmaskedCommercially marketed, soft, hydrogel contact lens with comfort additive for daily wear, daily disposable use. Blister pack label and lens packaging visible to participant. Lenses inserted and removed by participant.
DEVICEEtafilcon A contact lens with comfort additive (1DAVM), maskedCommercially marketed, soft, hydrogel contact lens for daily wear, daily disposable use. Blister pack label and packaging not visible to participant. Lenses inserted and removed by the investigator.
DEVICEEtafilcon A contact lens with comfort additive (1DAVM), partially maskedCommercially marketed, soft, hydrogel contact lens for daily wear, daily disposable use. Lens name and manufacturer on blister pack label concealed from participant. Lenses inserted and removed by the participant.

Timeline

Start date
2010-05-01
Primary completion
2011-02-01
Completion
2011-02-01
First posted
2010-07-02
Last updated
2012-07-10
Results posted
2012-05-15

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01155726. Inclusion in this directory is not an endorsement.