Clinical Trials Directory

Trials / Completed

CompletedNCT01412983

A Study to Evaluate the Product Feasibility of a New Silicone Hydrogel Contact Lens

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Bausch & Lomb Incorporated · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to determine the clinical feasibility and to evaluate the product performance of investigational contact lenses developed by Bausch + Lomb.

Conditions

Interventions

TypeNameDescription
DEVICEBausch & Lomb Test lensLens to be worn on a daily wear basis for one week. Participants will be provided with Bausch + Lomb renu® fresh™ multi-purpose solution for daily rinsing, cleaning, and disinfecting of their lenses.
DEVICECiba Vision soft contact lensLens to be worn on a daily wear basis for one week. Participants will be provided with Bausch + Lomb renu® fresh™ multi-purpose solution for daily rinsing, cleaning, and disinfecting of their lenses.

Timeline

Start date
2011-08-01
Primary completion
2011-09-01
Completion
2011-10-01
First posted
2011-08-09
Last updated
2014-04-29
Results posted
2014-04-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01412983. Inclusion in this directory is not an endorsement.