Clinical Trials Directory

Trials / Completed

CompletedNCT00349856

Dispensing Overnight Study in Lenses

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
40 (actual)
Sponsor
University of Waterloo · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to evaluate the fit and performance of an investigational soft contact lens in comparison with a currently marketed lens. Both lenses will be worn on a continuous wear basis, which means the lenses will be worn while sleeping.

Detailed description

The purpose of the study is to evaluate the fit and performance of an investigational soft contact lens in comparison with a currently marketed lens. Both lenses will be worn on a continuous wear basis, which means the lenses will be worn while sleeping. Physiological changes will be monitored and subjective ratings collected.

Conditions

Interventions

TypeNameDescription
DEVICEBiofinitySoft contact lens

Timeline

Start date
2005-01-01
Primary completion
2008-03-01
Completion
2008-03-01
First posted
2006-07-10
Last updated
2009-02-18

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00349856. Inclusion in this directory is not an endorsement.