Clinical Trials Directory

Trials / Completed

CompletedNCT02328937

Central Corneal Swelling With Silicone Hydrogel Materials

Daily Wear Central Corneal Swelling With Etafilcon A and 2 Silicone Hydrogel Materials

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
41 (actual)
Sponsor
Johnson & Johnson Vision Care, Inc. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This is a prospective, single site, unmasked, cross-over study with three silicone hydrogel contact lenses comparing central corneal swelling.

Conditions

Interventions

TypeNameDescription
DEVICEetafilcon Aspherical hydrophilic soft contact lens worn in a daily wear modality
DEVICElotrafilcon B
DEVICEcomfilcon A

Timeline

Start date
2014-11-01
Primary completion
2015-04-01
Completion
2015-04-01
First posted
2014-12-31
Last updated
2018-06-19
Results posted
2017-01-30

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02328937. Inclusion in this directory is not an endorsement.