Clinical Trials Directory

Trials / Completed

CompletedNCT02542072

Multi-Center Clinical Evaluation of Two Reusable Soft Contact Lenses

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
90 (actual)
Sponsor
CooperVision, Inc. · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the subjective performance of comfilcon A lens against samfilcon A lens after 4 weeks of reusable lens wear.

Detailed description

This will be a 90 subject, randomized, bilateral, subject-masked, dispensing, cross-over study comparing comfilcon A versus samfilcon A lenses over 8 weeks of daily wear (2 x 4-weeks). Both eyes will wear the same lens (test or control) for 4 weeks in a randomized fashion. Subjects will be masked to lens type and investigators will be masked to the lens codes.

Conditions

Interventions

TypeNameDescription
DEVICEcomfilcon Acontact lens
DEVICEsamfilcon Acontact lens

Timeline

Start date
2015-08-01
Primary completion
2016-02-01
Completion
2016-03-01
First posted
2015-09-04
Last updated
2017-10-24
Results posted
2017-03-21

Locations

5 sites across 2 countries: United States, United Kingdom

Source: ClinicalTrials.gov record NCT02542072. Inclusion in this directory is not an endorsement.