Clinical Trials Directory

Trials / Completed

CompletedNCT02588573

Overall Performance of a 1-day Silicone Hydrogel Lens When Habitual Soft Lens Wearers Are Refit

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
103 (actual)
Sponsor
CooperVision, Inc. · Industry
Sex
All
Age
17 Years
Healthy volunteers
Accepted

Summary

The objective of the study is to compare the overall subjective comfort profile over 8 hours of lens wear in two groups of habitual soft contact lens wearers (daily disposable hydrogel lenses and frequent replacement lenses) when refitted in to somofilcon A lenses.

Detailed description

This will be a prospective, single day, randomized, double-masked, non-dispensing, contralateral study. Participants were recruited into one of two groups - participants who habitually wore etafilcon A: daily disposable hydrogel lenses and participants who habitually wore frequent replacement lenses (FREQ).

Conditions

Interventions

TypeNameDescription
DEVICEetafilcon A (control)contact lens
DEVICEsomofilcon A (test)contact lens

Timeline

Start date
2015-10-01
Primary completion
2016-03-01
Completion
2016-04-01
First posted
2015-10-28
Last updated
2019-02-08
Results posted
2019-02-08

Locations

2 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT02588573. Inclusion in this directory is not an endorsement.