Clinical Trials Directory

Trials / Completed

CompletedNCT01464255

Comparative Study of Two Marketed 1-day Soft Contact Lenses

Clinical Performance of Ocufilcon D With a Wetting Agent to Ocufilcon B

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
71 (actual)
Sponsor
CooperVision, Inc. · Industry
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

This study is designed to evaluate ocufilcon D lens compared to ocufilcon B lens in a 1-week crossover, daily wear regimen.

Detailed description

This study is designed to evaluate 2 daily disposable contact lenses that are both currently cleared for the USA market. Study of the ocufilcon D lens compared to the ocufilcon B lens in a 1-week crossover, daily wear regimen. The primary objective is the comparison of fitting characteristics. The secondary objective is the comparison of comfort, end of day comfort and dryness measures.

Conditions

Interventions

TypeNameDescription
DEVICEocufilcon DParticipants wear a first pair of lenses for one week and then crossover and wear an alternate second pair of lenses for one week.
DEVICEocufilcon BParticipants wear a first pair of lenses for one week and then crossover and wear an alternate second pair of lenses for one week.

Timeline

Start date
2011-08-01
Primary completion
2011-10-01
Completion
2011-11-01
First posted
2011-11-03
Last updated
2014-08-19
Results posted
2014-08-19

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01464255. Inclusion in this directory is not an endorsement.