NCT01131130

Feasibility of a New Silicone Hydrogel Lens

A Study to Evaluate the Product Feasibility of a New Silicone Hydrogel Lens

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 120 (actual)
• Sponsor: Bausch & Lomb Incorporated · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The objective of this study is to determine the product feasibility of the investigational contact lens (Test) when compared to the currently marketed Acuvue Oasys contact lens (Control) and the Air Optix Aqua contact lens (Control) when worn by adapted wearers of soft contact lenses.

Conditions

• Myopia

Interventions

Type	Name	Description
DEVICE	Investigational contact lens	After one week of wearing the first lens type, the participants will crossover to the second lens type for one week, and then crossover to the third lens type.
DEVICE	Acuvue Oasys Contact Lens	After one week of wearing the first lens type, the participants will crossover to the second lens type for one week, and then crossover to the third lens type.
DEVICE	Air Optix Aqua	After one week of wearing the first lens type, the participants will crossover to the second lens type for one week, and then crossover to the third lens type.

Timeline

• Start date: 2010-05-01
• Primary completion: 2010-06-01
• Completion: 2010-06-01
• First posted: 2010-05-26
• Last updated: 2014-04-30
• Results posted: 2014-04-30

Locations

1 site across 1 country: United States