NCT00455455

Corneal and Conjunctival Sensitivity and Staining Study

• Status: Completed
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 50 (actual)
• Sponsor: University of Waterloo · Academic / Other
• Sex: All
• Age: 17 Years – 45 Years
• Healthy volunteers: Accepted

Summary

The primary objective of this study is to compare subjective symptoms and ocular health in a group of individuals who are currently wearing soft contact lenses on a daily wear basis, after a short period of no lens wear and during the time course when using differing care regimens.

Detailed description

The primary objective of this study is to compare subjective symptoms and ocular health in a group of individuals who are currently wearing soft contact lenses on a daily wear basis, after a short period of no lens wear and during the time course when using differing care regimens. Observations will be made to monitor physiology.

Conditions

• Myopia
• Hyperopia

Interventions

Type	Name	Description
DRUG	Optifree RepleniSH Multipurpose Disinfecting Solution	lens care system
DRUG	ReNu Multiplus Multipurpose Solution	lens care system

Timeline

• Start date: 2007-03-01
• Primary completion: 2008-12-01
• Completion: 2008-12-01
• First posted: 2007-04-03
• Last updated: 2010-07-12
• Results posted: 2010-07-12

Locations

1 site across 1 country: Canada