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CompletedNCT00661687

Comparative Performance of PureVision Lens Designs

A Study to Evaluate the Product Performance of the Redesigned Bausch & Lomb PureVision® Contact Lens (Test) Compared to the Currently Marketed Bausch & Lomb PureVision® Contact Lens (Control) When Worn on an Extended Wear Basis.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
206 (actual)
Sponsor
Bausch & Lomb Incorporated · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to evaluate the performance of the PureVision Lens designs when worn on a 30-day continuous wear basis

Conditions

Interventions

TypeNameDescription
DEVICECurrently Marketed PureVision Contact Lens.Contact lens for continuous wear
DEVICEAlternate Design of the PureVision Contact Lens.Contact lens for continuous wear

Timeline

Start date
2007-12-01
Primary completion
2008-02-01
Completion
2008-06-01
First posted
2008-04-18
Last updated
2011-12-12
Results posted
2010-10-15

Locations

2 sites across 2 countries: Malaysia, Philippines

Source: ClinicalTrials.gov record NCT00661687. Inclusion in this directory is not an endorsement.

Comparative Performance of PureVision Lens Designs (NCT00661687) · Clinical Trials Directory