Comparison of OPTI-FREE RepleniSH and ReNu Multi-Plus Lens Care Regimens on Corneal Epithelium

Not Applicable

Completed

• Conditions: Contact Lens Wear
• Interventions: Device: OPTI-FREE RepleniSH; Device: ReNu MultiPlus MPS

• Registration Number: NCT00724269
• Lead Sponsor: Alcon Research

Brief Summary

The purpose of this study is to evaluate the corneal epithelium after soft contact lens wear and use of two marketed multi-purpose solutions.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2008-07-25
• Study First Submitted QC: 2008-07-28
• Study First Posted: 2008-07-29
• Study Start: 2009-10
• Primary Completion: 2011-07
• Study Completion: 2011-07
• Status Verified: 2011-11
• Last Update Submitted: 2012-09-28
• Last Update Posted: 2012-10-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Successful contact lens wear on a daily wear basis
• Wear contact lenses at least 8 hours/day
• Vision correctable to at least 20/30
• Normal Eyes
• Other protocol-defined inclusion criteria may apply

Exclusion:

• Topical ocular medication use
• Other protocol-defined inclusion criteria may apply

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Opti Free RepliniSH	OPTI-FREE RepleniSH	Opti Free RepliniSH
ReNu Multi-Plus	ReNu MultiPlus MPS	ReNu Multi-Plus

Primary Outcome Measures

Name	Time	Method
Confocal microscopy analysis of Corneal Epithelium	2 weeks

Secondary Outcome Measures

Name	Time	Method
Patient comfort	2 weeks
Corneal Staining	2 weeks

Trial Locations

Locations (1)

Contact Alcon Call Center for Study Locations; 🇺🇸 Fort Worth, Texas, United States