NCT01118338

Evaluation of Two Different Designs of Bausch & Lomb Contact Lenses

A Study to Evaluate the Product Performance of Two Different Designs of Bausch & Lomb PureVision® Contact Lenses

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 376 (actual)
• Sponsor: Bausch & Lomb Incorporated · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The objective of this one month study is to evaluate the product performance of a redesigned PureVision Contact Lens compared to the PureVision Contact Lens when worn on a daily wear basis by wearers of contact lenses.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	Redesigned Purevision Contact Lens	Lenses will be dispensed at screening visit, subjects will wear lenses on a daily wear basis for one month.
DEVICE	PureVision Contact Lens	Lenses will be dispensed at screening visit, subjects will wear lenses on a daily wear basis for one month.

Timeline

• Start date: 2010-05-01
• Primary completion: 2010-06-01
• Completion: 2010-07-01
• First posted: 2010-05-06
• Last updated: 2020-10-06
• Results posted: 2020-10-06

Locations

1 site across 1 country: United States