NCT01391364

A Study to Evaluate a Modified Contact Lens

A Study to Evaluate the Product Performance of a Modified Contact Lens

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 438 (actual)
• Sponsor: Bausch & Lomb Incorporated · Industry
• Sex: All
• Age: 18 Years – 40 Years
• Healthy volunteers: Not accepted

Summary

This study is being conducted to evaluate the product performance of SofLens daily disposable contact lenses packaged in an investigational Test solution versus SofLens daily disposable contact lenses packaged in the currently marketed solution (Control), as it relates to comfort when worn by adapted soft contact lens wearers on a daily-wear basis.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	SofLens in investigational solution	SofLens in investigational solution, worn on a daily disposable basis for 7 days.
DEVICE	SofLens in currently marketed solution	SofLens packaged in currently marketed solution, worn on a daily disposable basis for 7 days.

Timeline

• Start date: 2011-04-01
• Primary completion: 2011-06-01
• Completion: 2011-07-01
• First posted: 2011-07-12
• Last updated: 2020-09-30
• Results posted: 2020-09-30

Locations

1 site across 1 country: United States