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A Study to Evaluate the Safety and Efficacy of a New Silicone Hydrogel Contact Lens Design

Myopia Clinical Trial

Official title:
A Study to Evaluate the Safety and Efficacy of a New Silicone Hydrogel Contact Lens Design

Clinical Trial Summary

The objective of this study is to evaluate the safety and efficacy of a new silicone hydrogel contact lens compared to the Bausch + Lomb PureVision contact lens when worn by adapted soft contact lens wearers.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01449526
Study type Interventional
Source Bausch & Lomb Incorporated
Contact
Status Completed
Phase N/A
Start date August 2011
Completion date January 2012
View Details
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