NCT01416142

A Study to Evaluate the Product Performance of the PureVision®2 High Definition (HD) Contact Lens

A Study to Evaluate the Product Performance of the PureVision®2 HD Contact Lens

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 63 (actual)
• Sponsor: Bausch & Lomb Incorporated · Industry
• Sex: All
• Age: 15 Years – 30 Years
• Healthy volunteers: Not accepted

Summary

The objective of this study is to evaluate the product performance of PureVision2 HD contact lenses.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	PureVision2 HD contact lenses	Lenses to be worn through 1/2 of an HD movie. Following the movie, all subjects were to wear the dispensed contact lenses on a daily wear basis for approximately one week.
DEVICE	Spectacles	Spectacles to be worn throughout 1/2 of an HD movie.

Timeline

• Start date: 2011-07-01
• Primary completion: 2011-08-01
• Completion: 2011-09-01
• First posted: 2011-08-12
• Last updated: 2013-12-25
• Results posted: 2013-12-25

Locations

1 site across 1 country: United States