Clinical Trials Directory

Trials / Completed

CompletedNCT02212301

Comparison of Two Marketed Lenses in a Controlled Environment

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
45 (actual)
Sponsor
Johnson & Johnson Vision Care, Inc. · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

This study is comparing two silicone hydrogel contact lenses in a controlled environment for identification of characteristics associated to vision.

Conditions

Interventions

TypeNameDescription
DEVICEsenofilcon AEach study contact lens will be worn as daily wear modality for a period of 2 weeks each.
DEVICElotrafilcon BEach study contact lens will be worn as daily wear modality for a period of 2 weeks each.

Timeline

Start date
2014-07-01
Primary completion
2014-12-01
Completion
2014-12-01
First posted
2014-08-08
Last updated
2016-10-28
Results posted
2016-09-27

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02212301. Inclusion in this directory is not an endorsement.